A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615906



Internal ID16403315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135587538..135590607hg38UCSC Ensembl
Innerchr9:138479384..138482453hg19UCSC Ensembl
Innerchr9:137619205..137622274hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383070
hg193070
hg183070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148227
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615906
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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