A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589214



Internal ID21537778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60393816..60405333hg38UCSC Ensembl
chr17:58471177..58482694hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3811518
hg1911518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088524
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589214
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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