A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936381



Internal ID24981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112136846..112137601hg38UCSC Ensembl
chr3:111855693..111856448hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556910
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936381
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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