A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564336



Internal ID16351745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35534330..35535285hg38UCSC Ensembl
Innerchr14:36003536..36004491hg19UCSC Ensembl
Innerchr14:35073287..35074242hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38956
hg19956
hg18956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3634n54
Supporting Variantsnssv825756
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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