A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv469n206



Internal ID22755773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:63604600..63846779hg38UCSC Ensembl
chr7:63064978..63307157hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38242180
hg19242180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141454, nsv6142509
Samples
Known GenesMIR4283-1, MIR4283-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv469n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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