A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479073



Internal ID21136626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22894456..22895099hg38UCSC Ensembl
chr14:23363665..23364308hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479073
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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