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dbVar

Database of genomic structural variation

nsv4426795

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:283,056

Links to Other Resources

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: 1023 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):67,706,963-67,990,018

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
nsv4426795	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	67,706,963	67,733,879	67,971,501	67,990,018
nsv4426795	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	67,474,434	67,501,350	67,738,972	67,757,489

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15718135	copy number loss	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15718135	Remapped	Perfect	NC_000011.10:g.(67 706963_67733879)_( 67971501_67990018) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	67,706,963	67,733,879	67,971,501	67,990,018
nssv15718135	Submitted genomic		NC_000011.9:g.(674 74434_67501350)_(6 7738972_67757489)d el	GRCh37 (hg19)		NC_000011.9	Chr11	67,474,434	67,501,350	67,738,972	67,757,489

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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