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dbVar

Database of genomic structural variation

nsv4413993

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:8,368

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: 161 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):39,528,849-39,537,216

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
nsv4413993	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	39,528,849	39,528,849	39,537,216	39,537,216
nsv4413993	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	40,019,489	40,019,489	40,027,856	40,027,856

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15726993	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
nssv15726993	Remapped	Perfect	NC_000019.10:g.(39 528849_39528849)_( 39537216_39537216) del	GRCh38.p12	First Pass	NC_000019.10	Chr19	39,528,849	39,528,849	39,537,216	39,537,216
nssv15726993	Submitted genomic		NC_000019.9:g.(400 19489_40019489)_(4 0027856_40027856)d el	GRCh37 (hg19)		NC_000019.9	Chr19	40,019,489	40,019,489	40,027,856	40,027,856

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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