A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613915



Internal ID16401324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25562456..25599997hg38UCSC Ensembl
Innerchr9:25562454..25599995hg19UCSC Ensembl
Innerchr9:25552454..25589995hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3837542
hg1937542
hg1837542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12614n54
Supporting Variantsnssv1156738
SamplesNINDS_213
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613915
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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