A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476183



Internal ID21133736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44907797..44912886hg38UCSC Ensembl
chr14:45377000..45382089hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg385090
hg195090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476183
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