A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613706



Internal ID16054429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17718920..18090936hg38UCSC Ensembl
Innerchr9:17718918..18090934hg19UCSC Ensembl
Innerchr9:17708918..18080934hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38372017
hg19372017
hg18372017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12582n54
Supporting Variantsnssv1129336
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613706
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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