A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519241



Internal ID295594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35928931..35929520hg38UCSC Ensembl
chr17:34255935..34256524hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712835
Samples
Known GenesRDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519241
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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