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dbVar

Database of genomic structural variation

nsv4410386

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:1,129

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: 135 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):99,949,646-99,950,774

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
nsv4410386	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	99,949,646	99,949,694	99,950,520	99,950,774
nsv4410386	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	100,870,803	100,870,851	100,871,677	100,871,931

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15734723	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
nssv15734723	Remapped	Perfect	NC_000004.12:g.(99 949646_99949694)_( 99950520_99950774) del	GRCh38.p12	First Pass	NC_000004.12	Chr4	99,949,646	99,949,694	99,950,520	99,950,774
nssv15734723	Submitted genomic		NC_000004.11:g.(10 0870803_100870851) _(100871677_100871 931)del	GRCh37 (hg19)		NC_000004.11	Chr4	100,870,803	100,870,851	100,871,677	100,871,931

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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