A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563922



Internal ID336847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10293273..10298894hg38UCSC Ensembl
chr2:10433399..10439020hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385622
hg195622
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563922
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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