A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931799



Internal ID21934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37399054..37400474hg38UCSC Ensembl
chr3:37440545..37441965hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381421
hg191421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438134
Supporting Variants
Samples
Known GenesC3orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005932


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