A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494528



Internal ID21152081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20212501..20238800hg38UCSC Ensembl
chr14:20680660..20706959hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826300
hg1926300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016539
Samples
Known GenesOR11H6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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