A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482935



Internal ID21140488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63643992..63645456hg38UCSC Ensembl
chr14:64110710..64112174hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381465
hg191465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482935
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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