A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485894



Internal ID21143447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82050799..82144385hg38UCSC Ensembl
chr14:82517143..82610729hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3893587
hg1993587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179660
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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