A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968330



Internal ID46207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68432043..68440204hg38UCSC Ensembl
chr5:67727870..67736031hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg388162
hg198162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460162
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968330
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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