A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579006



Internal ID20952077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44242224..44242913hg38UCSC Ensembl
chr15:44534422..44535111hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579006
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