A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238813



Internal ID20805853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64296312..64296645hg38UCSC Ensembl
chr15:64588511..64588844hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587442
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238813
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