A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565871



Internal ID16353280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101457586..101462048hg38UCSC Ensembl
Innerchr14:101923923..101928385hg19UCSC Ensembl
Innerchr14:100993676..100998138hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg384463
hg194463
hg184463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3919n54
Supporting Variantsnssv833705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565871
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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