A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603475



Internal ID16390884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65918786..66111599hg38UCSC Ensembl
Innerchr6:66628679..66821492hg19UCSC Ensembl
Innerchr6:66685400..66878213hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38192814
hg19192814
hg18192814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10733n54
Supporting Variantsnssv1153716
SamplesHGDP00571
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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