A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614133



Internal ID16401542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31842564..31879921hg38UCSC Ensembl
Innerchr9:31842562..31879919hg19UCSC Ensembl
Innerchr9:31832562..31869919hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3837358
hg1937358
hg1837358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12656n54
Supporting Variantsnssv1132821
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614133
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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