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dbVar

Database of genomic structural variation

nsv3117732

Organism: Homo sapiens

Study:nstd145 (Lu et al. 2017)
Variant Type:copy number variation
Method Type:Oligo aCGH
Submitted on:GRCh37 (hg19)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:4,491

Publication(s):Lu et al. 2017

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: 252 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):91,408,691-91,413,181

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3117732	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	91,408,691	91,413,181
nsv3117732	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	91,038,006	91,042,496

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14084273	deletion	sample143	Oligo aCGH	Probe signal intensity	95
nssv14084798	deletion	sample38	Oligo aCGH	Probe signal intensity	92

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv14084273	Remapped	Perfect	NC_000007.14:g.(?_ 91408691)_(9141318 1_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	91,408,691	91,413,181
nssv14084798	Remapped	Perfect	NC_000007.14:g.(?_ 91408691)_(9141318 1_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	91,408,691	91,413,181
nssv14084273	Submitted genomic		NC_000007.13:g.(?_ 91038006)_(9104249 6_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	91,038,006	91,042,496
nssv14084798	Submitted genomic		NC_000007.13:g.(?_ 91038006)_(9104249 6_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	91,038,006	91,042,496

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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