A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598881



Internal ID20971952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50938420..50938945hg38UCSC Ensembl
chr20:49554957..49555482hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4486n223
Supporting Variantsnssv18252618
Samples
Known GenesDPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598881
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