A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1130799



Internal ID15637299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21029331..21199681hg38UCSC Ensembl
Innerchr9:21029330..21199680hg19UCSC Ensembl
Innerchr9:21019330..21189680hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38170351
hg19170351
hg18170351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613752
Supporting Variants
Samples
Known GenesIFNA21, IFNA4, IFNB1, IFNW1, PTPLAD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1130799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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