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dbVar

Database of genomic structural variation

nsv6135669

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:9,000,010

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: 23283 SVs from 117 studies. See in: genome view

Remapped(Score: Perfect):50,174,166-59,174,175

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6135669	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	50,174,166	59,174,175
nsv6135669	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	49,470,000	58,470,001

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17680757	copy number loss	SAMN20524665	Sequencing	Paired-end mapping	405

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17680757	Remapped	Perfect	NC_000005.10:g.501 74166_59174175del	GRCh38.p12	First Pass	NC_000005.10	Chr5	50,174,166	59,174,175
nssv17680757	Submitted genomic		NC_000005.9:g.4947 0000_58470001del	GRCh37 (hg19)		NC_000005.9	Chr5	49,470,000	58,470,001

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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