A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563332



Internal ID336267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121190985..121204832hg38UCSC Ensembl
chr6:121512131..121525978hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3813848
hg1913848
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987571
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563332
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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