A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663816



Internal ID15400468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35333358..35352486hg38UCSC Ensembl
Innerchr14:35802564..35821692hg19UCSC Ensembl
Innerchr14:34872315..34891443hg18UCSC Ensembl
Innerchr14:34872315..34891443hg17UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3819129
hg1919129
hg1819129
hg1719129
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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