A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4971n223



Internal ID22807939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107692201..107700900hg38UCSC Ensembl
chr3:107411048..107419747hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6370142, nsv6359148, nsv6364972
Samples
Known GenesBBX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4971n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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