A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5814n223



Internal ID22808782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92181401..92212200hg38UCSC Ensembl
chr5:91477218..91508017hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3830800
hg1930800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6399810, nsv6403362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5814n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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