A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548105



Internal ID20921301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47505037..47505614hg38UCSC Ensembl
chr3:47546527..47547104hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262078
Samples
Known GenesELP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548105
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