A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257400



Internal ID20824440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:235159057..235164053hg38UCSC Ensembl
chr2:236067701..236072697hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg384997
hg194997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257400
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