A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492027



Internal ID21149580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56988701..56993600hg38UCSC Ensembl
chr14:57455419..57460318hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492027
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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