A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046244



Internal ID98630
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 StatusS
Merged Variantsnsv5558167
Supporting Variants
Samples
Known GenesTBC1D10C
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046244
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001405


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