A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7383n100



Internal ID22793470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5065360..5084214hg38UCSC Ensembl
chr9:5065360..5084214hg19UCSC Ensembl
chr9:5055360..5074214hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3818855
hg1918855
hg1818855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030821, nsv1027866, nsv1033735, nsv1017278, nsv1029234
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)dgv7383n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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