A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491137



Internal ID21148690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18223601..18427000hg38UCSC Ensembl
chr14:19000078..19203477hg19UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38203400
hg19203400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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