A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555034



Internal ID328202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75615855..75627475hg38UCSC Ensembl
chr13:76189991..76201611hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3811621
hg1911621
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691839
Samples
Known GenesLMO7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555034
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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