A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111553



Internal ID21294819
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 StatusM
Merged Variants
Supporting Variantsnssv14085385
Samplessample243
Known GenesCHCHD3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111553
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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