A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657762



Internal ID15394414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99616981..99683165hg38UCSC Ensembl
Innerchr14:100083318..100149502hg19UCSC Ensembl
Innerchr14:99153071..99219255hg18UCSC Ensembl
Innerchr14:99153071..99219255hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3866185
hg1966185
hg1866185
hg1766185
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519710
Supporting Variants
Samples
Known GenesHHIPL1, MIR5698
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657762
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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