A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420953



Internal ID200042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28854727..28854786hg38UCSC Ensembl
chr1:29181239..29181298hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900473
Samples
Known GenesOPRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420953
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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