A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194562



Internal ID20761602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32821067..32890851hg38UCSC Ensembl
chr14:33290273..33360057hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3869785
hg1969785
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476363
Supporting Variants
Samples
Known GenesAKAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194562
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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