A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025597



Internal ID19114815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5108562..5210671hg38UCSC Ensembl
Innerchr9:5108562..5210671hg19UCSC Ensembl
Innerchr9:5098562..5200671hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38102110
hg19102110
hg18102110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7384n100
Supporting Variantsnssv3758099
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)nsv1025597
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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