A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481931



Internal ID21139484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28262901..28267800hg38UCSC Ensembl
chr14:28732107..28737006hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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