A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603099



Internal ID16390508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:51334702..51340779hg38UCSC Ensembl
Innerchr6:51199500..51205577hg19UCSC Ensembl
Innerchr6:51307459..51313536hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg386078
hg196078
hg186078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1059006
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603099
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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