A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559846



Internal ID332867
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 StatusM
Merged Variants
Supporting Variantsnssv16927705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559846
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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