A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538996



Internal ID20912303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63020254..63021596hg38UCSC Ensembl
chr1:63485925..63487267hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538996
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