A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561715



Internal ID334685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80461269..80465568hg38UCSC Ensembl
chr1:80926954..80931253hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905697
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561715
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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