A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563142



Internal ID336079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224196051..224198246hg38UCSC Ensembl
chr1:224383753..224385948hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg382196
hg192196
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563142
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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