A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126534



Internal ID15633034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6032924..6332901hg38UCSC Ensembl
Innerchr9:6032924..6332901hg19UCSC Ensembl
Innerchr9:6022924..6322901hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38299978
hg19299978
hg18299978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613205
Supporting Variants
Samples
Known GenesIL33, TPD52L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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