A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155778



Internal ID15873364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94060175..94495560hg38UCSC Ensembl
Innerchr6:94769893..95205278hg19UCSC Ensembl
Innerchr6:94826614..95261999hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38435386
hg19435386
hg18435386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604170
Supporting Variants
SamplesHGDP00175
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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