A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936803



Internal ID25254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97837532..97842140hg38UCSC Ensembl
chr3:97556376..97560984hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384609
hg194609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442915
Supporting Variants
Samples
Known GenesCRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936803
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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