A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614569



Internal ID16055292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69476497..69519460hg38UCSC Ensembl
Innerchr9:72091413..72134376hg19UCSC Ensembl
Innerchr9:71281233..71324196hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3842964
hg1942964
hg1842964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176068
SamplesHGDP00464
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614569
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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