A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615255



Internal ID16055978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116695698..116728293hg38UCSC Ensembl
Innerchr9:119457977..119490572hg19UCSC Ensembl
Innerchr9:118497798..118530393hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3832596
hg1932596
hg1832596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141284
Samples
Known GenesASTN2, TRIM32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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