A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495027



Internal ID21152580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42691201..43032200hg38UCSC Ensembl
chr14:43160404..43501403hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38341000
hg19341000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2116n223
Supporting Variantsnssv18185474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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