A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582181



Internal ID20955252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72300756..72301003hg38UCSC Ensembl
chr15:72593097..72593344hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241874
Samples
Known GenesCELF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582181
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