A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493555



Internal ID270730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20752000..20768000hg38UCSC Ensembl
chr9:20751999..20767999hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17022440
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493555
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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