A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695478



Internal ID15432130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76619564..76642027hg38UCSC Ensembl
Innerchr14:77085907..77108370hg19UCSC Ensembl
Innerchr14:76155660..76178123hg18UCSC Ensembl
Innerchr14:76155660..76178123hg17UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3822464
hg1922464
hg1822464
hg1722464
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518067
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695478
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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