A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1129338



Internal ID15635838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17720177..18072087hg38UCSC Ensembl
Innerchr9:17720175..18072085hg19UCSC Ensembl
Innerchr9:17710175..18062085hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38351911
hg19351911
hg18351911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613708
Supporting Variants
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1129338
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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