A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260424



Internal ID20827464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155886075..155886330hg38UCSC Ensembl
chr3:155603864..155604119hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568228
Supporting Variants
Samples
Known GenesGMPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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