A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108174



Internal ID21292322
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 StatusS
Merged Variantsnsv3111495
Supporting Variants
Samplessample87
Known GenesCLCA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108174
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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