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dbVar

Database of genomic structural variation

nsv4426528

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:22,136

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: 87 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):60,070-82,205

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
nsv4426528	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	60,070	60,070	82,205	82,205
nsv4426528	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	60,070	60,070	82,205	82,205

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15710123	copy number gain	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
nssv15710123	Remapped	Perfect	NC_000019.10:g.(60 070_60070)_(82205_ 82205)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,070	60,070	82,205	82,205
nssv15710123	Submitted genomic		NC_000019.9:g.(600 70_60070)_(82205_8 2205)dup	GRCh37 (hg19)		NC_000019.9	Chr19	60,070	60,070	82,205	82,205

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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