A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111495



Internal ID21294761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86456177..86457965hg38UCSC Ensembl
Innerchr1:86921860..86923648hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg381789
hg191789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108174
Samplessample87
Known GenesCLCA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111495
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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