A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023491



Internal ID21932834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59394484..59394597hg38UCSC Ensembl
chr17:57471845..57471958hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621214
Samples
Known GenesYPEL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023491
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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