A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261067



Internal ID20828107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161386305..161956957hg38UCSC Ensembl
chr3:161104093..161674745hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38570653
hg19570653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562725
Supporting Variants
Samples
Known GenesLOC101243545, OTOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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