A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238136



Internal ID20805177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61865533..61865647hg38UCSC Ensembl
chr15:62157732..62157846hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576204
Supporting Variants
Samples
Known GenesVPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238136
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