A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594753



Internal ID20967824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64290855..64291325hg38UCSC Ensembl
chr15:64583054..64583524hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2564n223
Supporting Variantsnssv18238812
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594753
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