A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615145



Internal ID16402554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108413158..108760820hg38UCSC Ensembl
Innerchr9:111175438..111523100hg19UCSC Ensembl
Innerchr9:110215259..110562921hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38347663
hg19347663
hg18347663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176111
Samples1780862339_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615145
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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