A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599177



Internal ID20972248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47895820..48506748hg38UCSC Ensembl
chr20:46524564..47131704hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38610929
hg19607141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4475n223
Supporting Variantsnssv18252202
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599177
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