A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589606



Internal ID20962677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71302660..71303676hg38UCSC Ensembl
chr14:71769377..71770393hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2193n223
Supporting Variantsnssv18238597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589606
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