A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1069262



Internal ID15922448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98286772..98397213hg38UCSC Ensembl
Innerchr6:98734648..98845089hg19UCSC Ensembl
Innerchr6:98841369..98951810hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38110442
hg19110442
hg18110442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604252
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1069262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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