A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937906



Internal ID25987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107638150..107640692hg38UCSC Ensembl
chr3:107356997..107359539hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382543
hg192543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447495
Supporting Variants
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937906
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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