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dbVar

Database of genomic structural variation

nsv4382038

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:78,933

Publication(s):Zarrei et al. 2019

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: 1513 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):248,589,883-248,668,815

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4382038	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	248,589,883	248,668,815
nsv4382038	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	248,753,184	248,832,116

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15627734	copy number variation	1-0534-003	SNP array	Genotyping	16
nssv15698089	copy number variation	174929	SNP array	Genotyping	18

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15627734	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	248,589,883	248,668,815
nssv15698089	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	248,589,883	248,668,815
nssv15627734	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	248,753,184	248,832,116
nssv15698089	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	248,753,184	248,832,116

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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