A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017463



Internal ID19106680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5062473..5084578hg38UCSC Ensembl
Innerchr9:5062473..5084578hg19UCSC Ensembl
Innerchr9:5052473..5074578hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3822106
hg1922106
hg1822106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7382n100
Supporting Variantsnssv3692397
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)nsv1017463
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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