A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944488



Internal ID30333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194213721..194213722hg38UCSC Ensembl
chr3:193931510..193931511hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382
hg192
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944488
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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