A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577581



Internal ID16364990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70658460..71275327hg38UCSC Ensembl
Innerchr18:68325696..68942563hg19UCSC Ensembl
Innerchr18:66476676..67093543hg18UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38616868
hg19616868
hg18616868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150621
SamplesHGDP01228
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577581
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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