A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7384n100



Internal ID22793471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5097281..5228433hg38UCSC Ensembl
chr9:5097281..5228433hg19UCSC Ensembl
chr9:5087281..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 Variants
Supporting Variantsnsv1027127, nsv1024766, nsv1027432, nsv1025914, nsv1025597, nsv1026087, nsv1023933, nsv1034221, nsv1021124
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)dgv7384n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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