A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258002



Internal ID20825042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:44792635..44792912hg38UCSC Ensembl
chr2:45019774..45020051hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543552
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258002
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