A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483603



Internal ID21141156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71321187..71324186hg38UCSC Ensembl
chr14:71787904..71790903hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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