A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935990



Internal ID24706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85300376..85357603hg38UCSC Ensembl
chr3:85349526..85406753hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3857228
hg1957228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139802
Supporting Variants
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935990
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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