A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561143



Internal ID334129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90841764..90916508hg38UCSC Ensembl
chr13:91494018..91568762hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3874745
hg1974745
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694367
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561143
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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