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dbVar

Database of genomic structural variation

nsv6634987

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:82,598

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: 659 SVs from 77 studies. See in: genome view

Remapped(Score: Perfect):111,020,469-111,103,066

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv6634987	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	111,020,469	111,103,066
nsv6634987	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	111,672,816	111,755,413

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18327361	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
nssv18327361	Remapped	Perfect	NC_000013.11:g.(11 1020469_?)_(?_1111 03066)dup	GRCh38.p12	First Pass	NC_000013.11	Chr13	111,020,469	111,103,066
nssv18327361	Submitted genomic		NC_000013.10:g.(11 1672816_?)_(?_1117 55413)dup	GRCh37 (hg19)		NC_000013.10	Chr13	111,672,816	111,755,413

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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