A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528253



Internal ID304318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77627790..77656265hg38UCSC Ensembl
chr17:75623872..75652347hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3828476
hg1928476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528253
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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