A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615199



Internal ID16402608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112953875..112971402hg38UCSC Ensembl
Innerchr9:115716155..115733682hg19UCSC Ensembl
Innerchr9:114755976..114773503hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3817528
hg1917528
hg1817528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141243
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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