A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562018



Internal ID334982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9663210..9663278hg38UCSC Ensembl
chr11:9684757..9684825hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041278
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562018
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer