A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2803388



Internal ID15793248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62742010..63022038hg38UCSC Ensembl
Innerchr13:63316143..63596171hg19UCSC Ensembl
Innerchr13:62214144..62494172hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38280029
hg19280029
hg18280029
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514706
Supporting Variants
SamplesNA21453
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2803388
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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