A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592920



Internal ID20965991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56570916..56571711hg38UCSC Ensembl
chr14:57037634..57038429hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592920
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