A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494027



Internal ID21151580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51101574..51132592hg38UCSC Ensembl
chr14:51568292..51599310hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3831019
hg1931019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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