A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595488



Internal ID20968559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64026983..64154909hg38UCSC Ensembl
chr15:64319182..64447108hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38127927
hg19127927
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238798
Samples
Known GenesDAPK2, FAM96A, SNX1, SNX22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595488
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