A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937670



Internal ID25821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129533027..129533196hg38UCSC Ensembl
chr3:129251870..129252039hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438284
Supporting Variants
Samples
Known GenesRHO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937670
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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