A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692408



Internal ID18990689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5097281..5228433hg38UCSC Ensembl
Innerchr9:5097281..5228433hg19UCSC Ensembl
Innerchr9:5087281..5218433hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38131153
hg19131153
hg18131153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024766
Supporting Variants
Samples
Known GenesINSL6, JAK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3692408
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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