A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522833



Internal ID299091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34712994..34713055hg38UCSC Ensembl
chr20:33300798..33300859hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732121
Samples
Known GenesTP53INP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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