A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695091



Internal ID15431743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18659832..18673748hg38UCSC Ensembl
Innerchr3:18701324..18715240hg19UCSC Ensembl
Innerchr3:18676328..18690244hg18UCSC Ensembl
Innerchr3:18676328..18690244hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813917
hg1913917
hg1813917
hg1713917
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522311
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695091
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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