A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477027



Internal ID21134580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42036301..42050700hg38UCSC Ensembl
chr14:42505504..42519903hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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