A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567157



Internal ID20940228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181821917..181822850hg38UCSC Ensembl
chr3:181539705..181540638hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer