A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565671



Internal ID16353080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98886908..98908984hg38UCSC Ensembl
Innerchr14:99353245..99375321hg19UCSC Ensembl
Innerchr14:98422998..98445074hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3822077
hg1922077
hg1822077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148973
SamplesHGDP00721
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565671
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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