A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512093



Internal ID20885423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52791572..52795177hg38UCSC Ensembl
chr15:53083769..53087374hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383606
hg193606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512093
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