A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5778n223



Internal ID22808746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65917701..65951000hg38UCSC Ensembl
chr5:65213529..65246828hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3833300
hg1933300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413816, nsv6401993
Samples
Known GenesERBB2IP, LOC100303749
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5778n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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