A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614501



Internal ID16401910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41625832..41701115hg38UCSC Ensembl
Innerchr9:46095101..46170384hg19UCSC Ensembl
Innerchr9:45985097..46060380hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3875284
hg1975284
hg1875284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134680
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614501
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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