A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532615



Internal ID308534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50231801..50241457hg38UCSC Ensembl
chr17:48309162..48318818hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg389657
hg199657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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