A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2952381



Internal ID15665034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:93697864..93702112hg38UCSC Ensembl
Innerchr7:93327176..93331424hg19UCSC Ensembl
Innerchr7:93165112..93169360hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384249
hg194249
hg184249
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514433
Supporting Variants
SamplesNA18500
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2952381
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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