A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605491



Internal ID16392900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168623199..168642820hg38UCSC Ensembl
Innerchr6:169023879..169043500hg19UCSC Ensembl
Innerchr6:168765804..168785425hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3819622
hg1919622
hg1819622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155805
SamplesHGDP01049
Known GenesSMOC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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