A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930679



Internal ID21193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21788430..21824506hg38UCSC Ensembl
chr3:21829922..21865998hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3836077
hg1936077
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930679
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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