A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615384



Internal ID16402793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128647760..128651574hg38UCSC Ensembl
Innerchr9:131410039..131413853hg19UCSC Ensembl
Innerchr9:130449860..130453674hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383815
hg193815
hg183815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141640
Samples
Known GenesWDR34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615384
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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