A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697376



Internal ID15087342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:965228..1009238hg38UCSC Ensembl
Innerchr3:1006912..1050922hg19UCSC Ensembl
Innerchr3:981912..1025922hg18UCSC Ensembl
Innerchr3:981912..1025922hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3844011
hg1944011
hg1844011
hg1744011
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697376
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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