A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604334



Internal ID16391743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103019561..103129779hg38UCSC Ensembl
Innerchr6:103467436..103577654hg19UCSC Ensembl
Innerchr6:103574129..103684347hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38110219
hg19110219
hg18110219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070916
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604334
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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