A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582755



Internal ID20955826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:50526406..50527071hg38UCSC Ensembl
chr14:50993124..50993789hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2155n223
Supporting Variantsnssv18235329
Samples
Known GenesMAP4K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582755
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