A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000011



Internal ID67588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73731972..73732424hg38UCSC Ensembl
chr7:73146302..73146754hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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