A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940198



Internal ID27509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161368637..162525961hg38UCSC Ensembl
chr3:161086425..162243749hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381157325
hg191157325
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560984
Supporting Variants
Samples
Known GenesLOC101243545, OTOL1, SPTSSB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940198
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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