A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491785



Internal ID21149338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23885301..23900500hg38UCSC Ensembl
chr14:24354510..24369709hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3815200
hg1915200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2064n223
Supporting Variantsnssv18196369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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