A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968335



Internal ID46211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68580725..68594564hg38UCSC Ensembl
chr5:67876552..67890391hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3813840
hg1913840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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