A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529388



Internal ID305409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1506924..1896293hg38UCSC Ensembl
chr20:1487570..1876939hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38389370
hg19389370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730258
Samples
Known GenesLOC100289473, SIRPA, SIRPB1, SIRPD, SIRPG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529388
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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