A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565955



Internal ID16006678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102777002..102778060hg38UCSC Ensembl
Innerchr14:103243339..103244397hg19UCSC Ensembl
Innerchr14:102313092..102314150hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381059
hg191059
hg181059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3934n54
Supporting Variantsnssv834253, nssv834255, nssv834254
Samples
Known GenesTRAF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565955
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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