A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931366



Internal ID21660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29992070..29999973hg38UCSC Ensembl
chr3:30033561..30041464hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg387904
hg197904
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147148
Supporting Variants
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931366
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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