A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927705



Internal ID19178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194456250..194579035hg38UCSC Ensembl
chr2:195320974..195443759hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38122786
hg19122786
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559846
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927705
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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