A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605344



Internal ID16046067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167311162..167365010hg38UCSC Ensembl
Innerchr6:167724650..167778498hg19UCSC Ensembl
Innerchr6:167644640..167698488hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853849
hg1953849
hg1853849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154899
Samples1780854477_A
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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