A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564508



Internal ID16351917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41141953..41198356hg38UCSC Ensembl
Innerchr14:41611156..41667559hg19UCSC Ensembl
Innerchr14:40680906..40737309hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3856404
hg1956404
hg1856404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv827029, nssv827030, nssv827028, nssv827031
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564508
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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