A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615390



Internal ID16056113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128654590..128691724hg38UCSC Ensembl
Innerchr9:131416869..131454003hg19UCSC Ensembl
Innerchr9:130456690..130493824hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3837135
hg1937135
hg1837135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1143221
Samples
Known GenesSET, WDR34
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615390
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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