A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258929



Internal ID20825969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70183807..70185704hg38UCSC Ensembl
chr2:70410939..70412836hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381898
hg191898
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554170
Supporting Variants
Samples
Known GenesC2orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258929
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