A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603474



Internal ID16390883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65912453..65946204hg38UCSC Ensembl
Innerchr6:66622346..66656097hg19UCSC Ensembl
Innerchr6:66679067..66712818hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3833752
hg1933752
hg1833752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153715
Samples1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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