A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556674



Internal ID329805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21408802..21415059hg38UCSC Ensembl
chr8:21266313..21272570hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg386258
hg196258
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009238
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556674
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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