A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605338



Internal ID16046061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167158423..167420069hg38UCSC Ensembl
Innerchr6:167571911..167833557hg19UCSC Ensembl
Innerchr6:167491901..167753547hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38261647
hg19261647
hg18261647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154896
SamplesHGDP00929
Known GenesTCP10, TCP10L2, TTLL2, UNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605338
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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