A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019034



Internal ID19108251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5074582..5084696hg38UCSC Ensembl
Innerchr9:5074582..5084696hg19UCSC Ensembl
Innerchr9:5064582..5074696hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3810115
hg1910115
hg1810115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692407
Samples
Known GenesJAK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019034
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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