A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614536



Internal ID16401945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67899068..67918925hg38UCSC Ensembl
Innerchr9:67966514..67986371hg19UCSC Ensembl
Innerchr9:67556334..67576191hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3819858
hg1919858
hg1819858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134747
Samples
Known GenesANKRD20A1, ANKRD20A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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