A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935986



Internal ID24704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85298787..85391866hg38UCSC Ensembl
chr3:85347937..85441016hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3893080
hg1993080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436717
Supporting Variants
Samples
Known GenesCADM2, MIR5688
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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