A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539456



Internal ID20912751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220201546..220202135hg38UCSC Ensembl
chr1:220374888..220375477hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249268
Samples
Known GenesRAB3GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539456
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