A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493820



Internal ID21151373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21847221..22490499hg38UCSC Ensembl
chr14:22315403..22959487hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38643279
hg19644085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2060n223
Supporting Variantsnssv18016057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493820
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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