A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910778



Internal ID7953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33758463..34088562hg38UCSC Ensembl
chr2:33983530..34313629hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38330100
hg19330100
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910778
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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