A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613179



Internal ID16400588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5116616..5218524hg38UCSC Ensembl
Innerchr9:5116616..5218524hg19UCSC Ensembl
Innerchr9:5106616..5208524hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38101909
hg19101909
hg18101909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126511
Samples
Known GenesINSL6, JAK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613179
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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