A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615202



Internal ID16402611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112962042..112983376hg38UCSC Ensembl
Innerchr9:115724322..115745656hg19UCSC Ensembl
Innerchr9:114764143..114785477hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3821335
hg1921335
hg1821335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12852n54
Supporting Variantsnssv1141245
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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