A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564384



Internal ID16351793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37764288..37793557hg38UCSC Ensembl
Innerchr14:38233493..38262762hg19UCSC Ensembl
Innerchr14:37303244..37332513hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3829270
hg1929270
hg1829270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3643n54
Supporting Variantsnssv825978, nssv825979
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564384
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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