A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937679



Internal ID25828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129690987..129690987hg38UCSC Ensembl
chr3:129409830..129409830hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540426
Supporting Variants
Samples
Known GenesTMCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937679
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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