A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613888



Internal ID16401297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25155169..25282009hg38UCSC Ensembl
Innerchr9:25155167..25282007hg19UCSC Ensembl
Innerchr9:25145167..25272007hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38126841
hg19126841
hg18126841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132016
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613888
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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