A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566210



Internal ID16006933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105465248..105488368hg38UCSC Ensembl
Innerchr14:105931585..105954705hg19UCSC Ensembl
Innerchr14:105002630..105025750hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3823121
hg1923121
hg1823121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834810
Samples
Known GenesCRIP1, CRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566210
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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