A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563982



Internal ID336906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101929726..101931245hg38UCSC Ensembl
chr8:102941954..102943473hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381520
hg191520
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015748
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563982
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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