A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605341



Internal ID16046064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167210591..167365010hg38UCSC Ensembl
Innerchr6:167624079..167778498hg19UCSC Ensembl
Innerchr6:167544069..167698488hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38154420
hg19154420
hg18154420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11056n54
Supporting Variantsnssv1077045
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605341
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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