A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558167



Internal ID331239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67403713..67409210hg38UCSC Ensembl
chr11:67171184..67176681hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg385498
hg195498
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046244
Samples
Known GenesTBC1D10C
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558167
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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