A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590125



Internal ID20963196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57174286..57175261hg38UCSC Ensembl
chr16:57208198..57209173hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239314
Samples
Known GenesFAM192A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590125
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