A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698297



Internal ID15434949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34015906..34017533hg38UCSC Ensembl
Innerchr14:34485112..34486739hg19UCSC Ensembl
Innerchr14:33554863..33556490hg18UCSC Ensembl
Innerchr14:33554863..33556490hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381628
hg191628
hg181628
hg171628
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521678
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698297
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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