A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476268



Internal ID21133821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31521701..31573200hg38UCSC Ensembl
chr14:31990907..32042406hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3851500
hg1951500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178170
Samples
Known GenesNUBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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