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dbVar

Database of genomic structural variation

nsv6135886

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:350,002

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: 702 SVs from 57 studies. See in: genome view

Remapped(Score: Perfect):123,719,946-124,069,947

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6135886	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	123,719,946	124,069,947
nsv6135886	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	123,360,000	123,710,001

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17680446	copy number gain	SAMN20524664	Sequencing	Paired-end mapping	739

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17680446	Remapped	Perfect	NC_000007.14:g.123 719946_124069947du p	GRCh38.p12	First Pass	NC_000007.14	Chr7	123,719,946	124,069,947
nssv17680446	Submitted genomic		NC_000007.13:g.123 360000_123710001du p	GRCh37 (hg19)		NC_000007.13	Chr7	123,360,000	123,710,001

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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