A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564339



Internal ID16351748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35534787..35535507hg38UCSC Ensembl
Innerchr14:36003993..36004713hg19UCSC Ensembl
Innerchr14:35073744..35074464hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38721
hg19721
hg18721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3635n54
Supporting Variantsnssv825763, nssv825762
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564339
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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