A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987581



Internal ID59159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121226945..121226947hg38UCSC Ensembl
chr6:121548091..121548093hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383
hg193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558581
Supporting Variants
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987581
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.019669


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