A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604085



Internal ID16391494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80588173..80730256hg38UCSC Ensembl
Innerchr6:81297890..81439973hg19UCSC Ensembl
Innerchr6:81354609..81496692hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38142084
hg19142084
hg18142084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1067372
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604085
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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