A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611489



Internal ID16398898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:70986138..71051176hg38UCSC Ensembl
Innerchr8:71898373..71963411hg19UCSC Ensembl
Innerchr8:72060927..72125965hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3865039
hg1965039
hg1865039
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12190n54
Supporting Variantsnssv1156858
SamplesHGDP00635
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611489
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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