nsv1156204

Organism: Homo sapiens

Study:nstd97 (Lou et al. 2014)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:16
Validation:Not tested
Clinical Assertions: No
Region Size:17,335

Publication(s):Lou et al. 2014

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 248 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):97,250,644-97,267,978

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv1156204	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nsv1156204	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv4014731	deletion	SNP array	SNP genotyping analysis	1
nssv4014732	deletion	SNP array	SNP genotyping analysis	1
nssv4014733	duplication	SNP array	SNP genotyping analysis	3
nssv4014734	deletion	SNP array	SNP genotyping analysis	1
nssv4015378	deletion	SNP array	SNP genotyping analysis	0
nssv4015379	deletion	SNP array	SNP genotyping analysis	1
nssv4015380	deletion	SNP array	SNP genotyping analysis	1
nssv4015381	deletion	SNP array	SNP genotyping analysis	1
nssv4015382	deletion	SNP array	SNP genotyping analysis	1
nssv4015383	deletion	SNP array	SNP genotyping analysis	1
nssv4015384	deletion	SNP array	SNP genotyping analysis	1
nssv4015385	deletion	SNP array	SNP genotyping analysis	1
nssv4015386	deletion	SNP array	SNP genotyping analysis	1
nssv4015387	deletion	SNP array	SNP genotyping analysis	0
nssv4015388	deletion	SNP array	SNP genotyping analysis	1
nssv4015389	deletion	SNP array	SNP genotyping analysis	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv4014731	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4014732	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4014733	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4014734	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015378	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015379	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015380	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015381	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015382	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015383	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015384	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015385	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015386	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015387	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015388	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4015389	Remapped	Perfect	NC_000004.12:g.(97 250644_97251263)_( 97263981_97267978) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,250,644	97,251,263	97,263,981	97,267,978
nssv4014731	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4014732	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4014733	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) dup	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4014734	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015378	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015379	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015380	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015381	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015382	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015383	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015384	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015385	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015386	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015387	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015388	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129
nssv4015389	Submitted genomic		NC_000004.11:g.(98 171795_98172414)_( 98185132_98189129) del	GRCh37 (hg19)		NC_000004.11	Chr4	98,171,795	98,172,414	98,185,132	98,189,129

dbVar

Database of genomic structural variation

nsv1156204

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant