A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542864



Internal ID20916115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92319770..92320523hg38UCSC Ensembl
chr1:92785327..92786080hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252681
Samples
Known GenesRPAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542864
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