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dbVar

Database of genomic structural variation

nsv499755

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:69,228

Publication(s):Kidd et al. 2010

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: 2620 SVs from 97 studies. See in: genome view

Remapped(Score: Perfect):78,257,474-78,326,701

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499755	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	78,257,474	78,326,701
nsv499755	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	78,967,191	79,036,418
nsv499755	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000006.10	Chr6	79,023,910	79,093,137

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585992	copy number loss	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585992	Remapped	Perfect	NC_000006.12:g.782 57474_78326701del	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,257,474	78,326,701
nssv585992	Remapped	Perfect	NC_000006.11:g.789 67191_79036418del	GRCh37.p13	First Pass	NC_000006.11	Chr6	78,967,191	79,036,418
nssv585992	Submitted genomic		NC_000006.10:g.790 23910_79093137del	NCBI36 (hg18)		NC_000006.10	Chr6	79,023,910	79,093,137

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

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