A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525834



Internal ID301983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71685231..71689199hg38UCSC Ensembl
chr17:69681372..69685340hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383969
hg193969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17714394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525834
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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