A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604561



Internal ID16391970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119993717..120103739hg38UCSC Ensembl
Innerchr6:120314863..120424885hg19UCSC Ensembl
Innerchr6:120356562..120466584hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38110023
hg19110023
hg18110023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1072352
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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