A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503879



Internal ID20877137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81979080..81981010hg38UCSC Ensembl
chr15:82271421..82273351hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381931
hg191931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer