A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535743



Internal ID20909097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51501288..51501668hg38UCSC Ensembl
chr1:51966960..51967340hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251670
Samples
Known GenesEPS15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535743
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