A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512006



Internal ID20885336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52639417..52665065hg38UCSC Ensembl
chr15:52931614..52957262hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3825649
hg1925649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024077
Samples
Known GenesFAM214A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512006
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