A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525472



Internal ID301631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1777138..1777192hg38UCSC Ensembl
chr20:1757784..1757838hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730276
Samples
Known GenesLOC100289473
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525472
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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