A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613702



Internal ID16401111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17583312..17630593hg38UCSC Ensembl
Innerchr9:17583310..17630591hg19UCSC Ensembl
Innerchr9:17573310..17620591hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3847282
hg1947282
hg1847282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12581n54
Supporting Variantsnssv1129330
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613702
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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