A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685662



Internal ID15422314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98816953..98828161hg38UCSC Ensembl
Innerchr14:99283290..99294498hg19UCSC Ensembl
Innerchr14:98353043..98364251hg18UCSC Ensembl
Innerchr14:98353043..98364251hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3811209
hg1911209
hg1811209
hg1711209
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516383
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685662
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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