A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934875



Internal ID23982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61492598..61507130hg38UCSC Ensembl
chr3:61478272..61492804hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3814533
hg1914533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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