A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492655



Internal ID21150208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49901725..49908676hg38UCSC Ensembl
chr14:50368443..50375394hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg386952
hg196952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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