A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559026



Internal ID332072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76198008..76208384hg38UCSC Ensembl
chr13:76772144..76782520hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3810377
hg1910377
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559026
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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