A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252815



Internal ID20819855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9937585..9938330hg38UCSC Ensembl
chr1:9997643..9998388hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548533
Supporting Variants
Samples
Known GenesLZIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252815
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