A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568139



Internal ID20941210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47515129..47515944hg38UCSC Ensembl
chr4:47517146..47517961hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5262n223
Supporting Variantsnssv18266350
Samples
Known GenesATP10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568139
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