A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046194



Internal ID98595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66496422..66496543hg38UCSC Ensembl
chr11:66263893..66264014hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498281
Supporting Variants
Samples
Known GenesDPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046194
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003278


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