A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085385



Internal ID21276864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132883579..132900273hg38UCSC Ensembl
Innerchr7:132568339..132585033hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3816695
hg1916695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111553
Supporting Variants
Samplessample243
Known GenesCHCHD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085385
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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