A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614579



Internal ID16055302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69487853..69499585hg38UCSC Ensembl
Innerchr9:72102769..72114501hg19UCSC Ensembl
Innerchr9:71292589..71304321hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3811733
hg1911733
hg1811733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137121
Samples
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614579
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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