A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560450



Internal ID333457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44978382..44981689hg38UCSC Ensembl
chr2:45205521..45208828hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg383308
hg193308
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16913576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560450
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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