A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613695



Internal ID16054418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17273733..17348414hg38UCSC Ensembl
Innerchr9:17273731..17348412hg19UCSC Ensembl
Innerchr9:17263731..17338412hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3874682
hg1974682
hg1874682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129323
Samples
Known GenesCNTLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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