A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570111



Internal ID20943182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77699018..77699206hg38UCSC Ensembl
chr5:76994843..76995031hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270248
Samples
Known GenesTBCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570111
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