A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595520



Internal ID20968591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50073559..51225509hg38UCSC Ensembl
chr15:50365756..51517706hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381151951
hg191151951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238076
Samples
Known GenesAP4E1, ATP8B4, CYP19A1, DCAF13P3, FLJ10038, GABPB1, GABPB1-AS1, HDC, MIR4712, SLC27A2, SPPL2A, TNFAIP8L3, TRPM7, USP50, USP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595520
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