A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613690



Internal ID16401099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16941008..16984997hg38UCSC Ensembl
Innerchr9:16941006..16984995hg19UCSC Ensembl
Innerchr9:16931006..16974995hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3843990
hg1943990
hg1843990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12580n54
Supporting Variantsnssv1129320
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613690
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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