A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613914



Internal ID16401323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25562456..25598676hg38UCSC Ensembl
Innerchr9:25562454..25598674hg19UCSC Ensembl
Innerchr9:25552454..25588674hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3836221
hg1936221
hg1836221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12614n54
Supporting Variantsnssv1156737, nssv1156736
SamplesHGDP00267, NINDS_156
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613914
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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