A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17048403



Internal ID100141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82882496..82882794hg38UCSC Ensembl
chr11:82593538..82593836hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505693
Supporting Variants
Samples
Known GenesPRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17048403
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.016703


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