A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025914



Internal ID19115131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5106023..5214002hg38UCSC Ensembl
Innerchr9:5106023..5214002hg19UCSC Ensembl
Innerchr9:5096023..5204002hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38107980
hg19107980
hg18107980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7384n100
Supporting Variantsnssv3758098
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)nsv1025914
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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