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dbVar

Database of genomic structural variation

nsv4375018

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:141,226

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: 691 SVs from 78 studies. See in: genome view

Submitted genomic98,025,640-98,166,865

Variant Region Placement Information

Variant Region ID	Placement Type	Assembly	Assembly Unit	Sequence ID	Chr	Inner Start	Inner Stop
nsv4375018	Submitted genomic	GRCh37 (hg19)	Primary Assembly	NC_000002.11	Chr2	98,025,640	98,166,865

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15692650	copy number loss	OCD69-896071	SNP array	Genotyping	22
nssv15702957	copy number loss	237508	SNP array	Genotyping	39

Variant Call Placement Information

Variant Call ID	Placement Type	HGVS	Assembly	Sequence ID	Chr	Inner Start	Inner Stop
nssv15692650	Submitted genomic	NC_000002.11:g.(?_ 98025640)_(9816686 5_?)del	GRCh37 (hg19)	NC_000002.11	Chr2	98,025,640	98,166,865
nssv15702957	Submitted genomic	NC_000002.11:g.(?_ 98025640)_(9816686 5_?)del	GRCh37 (hg19)	NC_000002.11	Chr2	98,025,640	98,166,865

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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