A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552460



Internal ID20925588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44759912..44760646hg38UCSC Ensembl
chr3:44801404..44802138hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260731
Samples
Known GenesKIAA1143
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552460
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