A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613757



Internal ID16054480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21289924..21316650hg38UCSC Ensembl
Innerchr9:21289923..21316649hg19UCSC Ensembl
Innerchr9:21279923..21306649hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3826727
hg1926727
hg1826727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1130802
Samples
Known GenesIFNA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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