A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560984



Internal ID333973
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 StatusM
Merged Variants
Supporting Variantsnssv16940198
Samples
Known GenesLOC101243545, OTOL1, SPTSSB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560984
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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