A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000462



Internal ID67886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98026214..98028333hg38UCSC Ensembl
chr7:97655526..97657645hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382120
hg192120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141480
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000462
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.116787


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