A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2091n223



Internal ID22805059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33470401..33537500hg38UCSC Ensembl
chr14:33939607..34006706hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3867100
hg1967100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6491317, nsv6477943, nsv6487820, nsv6476715
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2091n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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