A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023933



Internal ID19113150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5116616..5219889hg38UCSC Ensembl
Innerchr9:5116616..5219889hg19UCSC Ensembl
Innerchr9:5106616..5209889hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38103274
hg19103274
hg18103274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7384n100
Supporting Variantsnssv3692415
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)nsv1023933
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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