A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265748



Internal ID20832788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33703554..33704300hg38UCSC Ensembl
chr4:33705176..33705922hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265748
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