A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484457



Internal ID21142010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61173807..61176187hg38UCSC Ensembl
chr14:61640525..61642905hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382381
hg192381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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