A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1071659



Internal ID15924845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104449043..104496724hg38UCSC Ensembl
Innerchr6:104896918..104944599hg19UCSC Ensembl
Innerchr6:105003611..105051292hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3847682
hg1947682
hg1847682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604394
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)nssv1071659
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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