A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555397



Internal ID328554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66593877..66594706hg38UCSC Ensembl
chr11:66361348..66362177hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046203
Samples
Known GenesCCS
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555397
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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