A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561185



Internal ID334171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26484815..26512108hg38UCSC Ensembl
chr13:27058952..27086245hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3827294
hg1927294
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561185
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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