A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937881



Internal ID25968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107130765..107146278hg38UCSC Ensembl
chr3:106849612..106865125hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3815514
hg1915514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437553
Supporting Variants
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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