A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532393



Internal ID308317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65217072..65217168hg38UCSC Ensembl
chr17:63213190..63213286hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714119
Samples
Known GenesRGS9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532393
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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