A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265521



Internal ID20832561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1935582..1937279hg38UCSC Ensembl
chr4:1937309..1939006hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561040
Supporting Variants
Samples
Known GenesWHSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265521
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