A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584974



Internal ID20958045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:93987282..93988957hg38UCSC Ensembl
chr13:94639536..94641211hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219584
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584974
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