A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475991



Internal ID21133544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83082641..83190811hg38UCSC Ensembl
chr14:83548985..83657155hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38108171
hg19108171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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