A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490789



Internal ID21148342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60218935..60227360hg38UCSC Ensembl
chr14:60685653..60694078hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388426
hg198426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020483
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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