A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564567



Internal ID16351976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42368294..42492102hg38UCSC Ensembl
Innerchr14:42837497..42961305hg19UCSC Ensembl
Innerchr14:41907247..42031055hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38123809
hg19123809
hg18123809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827226
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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