A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543764



Internal ID20917010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24529408..24529771hg38UCSC Ensembl
chr1:24855898..24856261hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251436
Samples
Known GenesRCAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543764
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