A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2951678



Internal ID15730648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79842380..79852124hg38UCSC Ensembl
Innerchr7:79471696..79481440hg19UCSC Ensembl
Innerchr7:79309632..79319376hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg389745
hg199745
hg189745
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514428
Supporting Variants
SamplesNA19103
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2951678
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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