A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486752



Internal ID21144305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43392501..43702300hg38UCSC Ensembl
chr14:43861704..44171503hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38309800
hg19309800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2117n223
Supporting Variantsnssv18195549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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