A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910620



Internal ID7853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26903123..26903186hg38UCSC Ensembl
chr2:27125991..27126054hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436428
Supporting Variants
Samples
Known GenesDPYSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910620
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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