A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544852



Internal ID20918090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231217402..231217984hg38UCSC Ensembl
chr2:232082115..232082697hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257318
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544852
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