A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615900



Internal ID16403309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135587331..135588640hg38UCSC Ensembl
Innerchr9:138479177..138480486hg19UCSC Ensembl
Innerchr9:137618998..137620307hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381310
hg191310
hg181310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12988n54
Supporting Variantsnssv1148212, nssv1148211
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615900
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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