A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691573



Internal ID15081539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4124049..4232962hg38UCSC Ensembl
Innerchr3:4165733..4274646hg19UCSC Ensembl
Innerchr3:4140733..4249646hg18UCSC Ensembl
Innerchr3:4140733..4249646hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38108914
hg19108914
hg18108914
hg17108914
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691573
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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