A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523865



Internal ID300083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69602779..69608091hg38UCSC Ensembl
chr17:67598920..67604232hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg385313
hg195313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523865
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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