A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490020



Internal ID21147573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39778645..39880657hg38UCSC Ensembl
chr14:40247849..40349861hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38102013
hg19102013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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