A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258755



Internal ID20825795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63423036..63884116hg38UCSC Ensembl
chr2:63650171..64111250hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38461081
hg19461080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544568
Supporting Variants
Samples
Known GenesMDH1, UGP2, WDPCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258755
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