A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155092



Internal ID15875431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102992625..103769899hg38UCSC Ensembl
Innerchr6:103440500..104217774hg19UCSC Ensembl
Innerchr6:103547193..104324467hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38777275
hg19777275
hg18777275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604333
Supporting Variants
SamplesHGDP00683
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155092
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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