A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480397



Internal ID21137950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34212601..34218300hg38UCSC Ensembl
chr14:34681807..34687506hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192437
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480397
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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