A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517683



Internal ID15444976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72656563..72671481hg38UCSC Ensembl
Innerchr14:73123271..73138189hg19UCSC Ensembl
Innerchr14:72193024..72207942hg18UCSC Ensembl
Innerchr14:72193024..72207942hg17UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3814919
hg1914919
hg1814919
hg1714919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv676737, nssv692204, nssv663722, nssv652836, nssv670777, nssv660176, nssv672616, nssv656775, nssv681826, nssv687397, nssv687150
Samples
Known GenesDPF3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517683
Frequency
Sample Size2026
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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