A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477120



Internal ID21134673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62284459..62682628hg38UCSC Ensembl
chr14:62751177..63149346hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38398170
hg19398170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477120
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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