A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559108



Internal ID332152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87680339..87681640hg38UCSC Ensembl
chr13:88332594..88333895hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559108
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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