A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412276



Internal ID21069829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59079532..59093265hg38UCSC Ensembl
chr5:58375359..58389092hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3813734
hg1913734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134323
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412276
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