A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532878



Internal ID308790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38678998..38681272hg38UCSC Ensembl
chr17:36835251..36837525hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382275
hg192275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532878
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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