A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027127



Internal ID19116346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5108562..5222613hg38UCSC Ensembl
Innerchr9:5108562..5222613hg19UCSC Ensembl
Innerchr9:5098562..5212613hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38114052
hg19114052
hg18114052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7384n100
Supporting Variantsnssv3692412
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)nsv1027127
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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