A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541284



Internal ID20914565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38822326..38823830hg38UCSC Ensembl
chr2:39049468..39050972hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg381505
hg191505
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260211
Samples
Known GenesDHX57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541284
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer