A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615987



Internal ID16056710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136939743..136947810hg38UCSC Ensembl
Innerchr9:139834195..139842262hg19UCSC Ensembl
Innerchr9:138954016..138962083hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388068
hg198068
hg188068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148339
Samples
Known GenesC8G, FBXW5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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