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dbVar

Database of genomic structural variation

nsv6635916

Organism: Homo sapiens

Study:nstd227 (Kikas et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:148,999

Publication(s):Kikas et al. 2023

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: 1349 SVs from 102 studies. See in: genome view

Remapped(Score: Perfect):135,257,320-135,406,318

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6635916	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	135,257,320	135,406,318
nsv6635916	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	138,149,166	138,298,164

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18326907	duplication	SNP array	Probe signal intensity
nssv18326908	duplication	SNP array	Probe signal intensity
nssv18326909	duplication	SNP array	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18326907	Remapped	Perfect	NC_000009.12:g.(13 5257320_?)_(?_1354 06318)dup	GRCh38.p12	First Pass	NC_000009.12	Chr9	135,257,320	135,406,318
nssv18326908	Remapped	Perfect	NC_000009.12:g.(13 5257320_?)_(?_1354 06318)dup	GRCh38.p12	First Pass	NC_000009.12	Chr9	135,257,320	135,406,318
nssv18326909	Remapped	Perfect	NC_000009.12:g.(13 5257320_?)_(?_1354 06318)dup	GRCh38.p12	First Pass	NC_000009.12	Chr9	135,257,320	135,406,318
nssv18326907	Submitted genomic		NC_000009.11:g.(13 8149166_?)_(?_1382 98164)dup	GRCh37 (hg19)		NC_000009.11	Chr9	138,149,166	138,298,164
nssv18326908	Submitted genomic		NC_000009.11:g.(13 8149166_?)_(?_1382 98164)dup	GRCh37 (hg19)		NC_000009.11	Chr9	138,149,166	138,298,164
nssv18326909	Submitted genomic		NC_000009.11:g.(13 8149166_?)_(?_1382 98164)dup	GRCh37 (hg19)		NC_000009.11	Chr9	138,149,166	138,298,164

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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