A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613178



Internal ID16400587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5098223..5267043hg38UCSC Ensembl
Innerchr9:5098223..5267043hg19UCSC Ensembl
Innerchr9:5088223..5257043hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38168821
hg19168821
hg18168821
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156212
SamplesNINDS_223
Known GenesINSL4, INSL6, JAK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613178
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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