A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023851



Internal ID21933194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59394419..59394536hg38UCSC Ensembl
chr17:57471780..57471897hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632868
Samples
Known GenesYPEL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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