A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596398



Internal ID20969469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36659612..36660084hg38UCSC Ensembl
chr20:35288015..35288487hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252554
Samples
Known GenesNDRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596398
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