A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563185



Internal ID336122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46388537..46391007hg38UCSC Ensembl
chr11:46410087..46412557hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382471
hg192471
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563185
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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