A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600978



Internal ID16388387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10335252..10358462hg38UCSC Ensembl
Innerchr6:10335485..10358695hg19UCSC Ensembl
Innerchr6:10443471..10466681hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3823211
hg1923211
hg1823211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1049397
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600978
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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