A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699162



Internal ID15089128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17394538..17454801hg38UCSC Ensembl
Innerchr9:17394536..17454799hg19UCSC Ensembl
Innerchr9:17384536..17444799hg18UCSC Ensembl
Innerchr9:17384536..17444799hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3860264
hg1960264
hg1860264
hg1760264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523411
Supporting Variants
Samples
Known GenesCNTLN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699162
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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