A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562725



Internal ID20935796
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 StatusM
Merged Variants
Supporting Variantsnssv18261067
Samples
Known GenesLOC101243545, OTOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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