A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488303



Internal ID21145856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77156378..77156972hg38UCSC Ensembl
chr14:77622721..77623315hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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