A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540728



Internal ID20914018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231199884..231200523hg38UCSC Ensembl
chr2:232064598..232065237hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257317
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540728
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