A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564462



Internal ID16351871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40460102..40479184hg38UCSC Ensembl
Innerchr14:40929306..40948388hg19UCSC Ensembl
Innerchr14:39999056..40018138hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3819083
hg1919083
hg1819083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148697
SamplesHGDP01030
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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