A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024766



Internal ID19113983
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 StatusM
Merged Variantsdgv7384n100
Supporting Variantsnssv3692408, nssv3692409
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)nsv1024766
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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