A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404859



Internal ID21062412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13580921..13592055hg38UCSC Ensembl
chr6:13581153..13592287hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3811135
hg1911135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139520
Samples
Known GenesSIRT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404859
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