A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526672



Internal ID302793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65177039..65177496hg38UCSC Ensembl
chr17:63173157..63173614hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714115
Samples
Known GenesRGS9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526672
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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