A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558876



Internal ID331928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86400700..86407362hg38UCSC Ensembl
chr10:88160457..88167119hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg386663
hg196663
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558876
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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