A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734895



Internal ID158561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99832570..99832733hg38UCSC Ensembl
chr3:99551414..99551577hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452439
Supporting Variants
Samples
Known GenesCMSS1, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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