A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566256



Internal ID16353665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474383..105488519hg38UCSC Ensembl
Innerchr14:105940720..105954856hg19UCSC Ensembl
Innerchr14:105011765..105025901hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3814137
hg1914137
hg1814137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3996n54
Supporting Variantsnssv834918
Samples
Known GenesCRIP1, CRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566256
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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