A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565886



Internal ID16353295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101702580..101713702hg38UCSC Ensembl
Innerchr14:102168917..102180039hg19UCSC Ensembl
Innerchr14:101238670..101249792hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3811123
hg1911123
hg1811123
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833734, nssv833732, nssv833733, nssv833731, nssv833735, nssv833736
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565886
Frequency
Sample Size17421
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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