A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479106



Internal ID21136659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21765668..21857377hg38UCSC Ensembl
chr14:22233906..22325554hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3891710
hg1991649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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