A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705912



Internal ID15442564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36408496..36420367hg38UCSC Ensembl
Innerchr14:36877701..36889572hg19UCSC Ensembl
Innerchr14:35947452..35959323hg18UCSC Ensembl
Innerchr14:35947452..35959323hg17UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3811872
hg1911872
hg1811872
hg1711872
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522537
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705912
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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