A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146396



Internal ID345601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35928297..35928349hg38UCSC Ensembl
chr20:34516219..34516271hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732172
Samples
Known GenesPHF20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146396
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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