A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490610



Internal ID21148163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21898001..22246100hg38UCSC Ensembl
chr14:22366181..22713984hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38348100
hg19347804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490610
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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