A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261895



Internal ID20828935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19471110..19477906hg38UCSC Ensembl
chr3:19512602..19519398hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551759
Supporting Variants
Samples
Known GenesKCNH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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