A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559265



Internal ID20932336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83603811..83604364hg38UCSC Ensembl
chr4:84524964..84525517hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266056
Samples
Known GenesAGPAT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559265
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