A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588574



Internal ID20961645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49590248..49590810hg38UCSC Ensembl
chr14:50056966..50057528hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225485
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588574
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