A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586767



Internal ID20959838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40615653..40616063hg38UCSC Ensembl
chr15:40907851..40908261hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238258
Samples
Known GenesCASC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586767
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