A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574286



Internal ID20947357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68852162..69022296hg38UCSC Ensembl
chr4:69717880..69888014hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38170135
hg19170135
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5311n223
Supporting Variantsnssv18265912
Samples
Known GenesUGT2A3, UGT2B10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574286
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