A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv468734



Internal ID15041042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888169..29926574hg38UCSC Ensembl
Innerchr6:29961770..30000151hg16UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3838406
hg1638382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437962
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisHardy-Weinberg disequilibrium - we looked for genomic regions in which hetobs/hetexp consistency fell below some cutoff (we used cutoffs of 0.7 and 0.4).
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nssv468734
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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