A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1063578



Internal ID15916764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68092182..68202362hg38UCSC Ensembl
Innerchr6:68802074..68912254hg19UCSC Ensembl
Innerchr6:68858795..68968975hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38110181
hg19110181
hg18110181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603606
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)nssv1063578
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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