A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032488



Internal ID21941831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50350142..50350534hg38UCSC Ensembl
chr17:48427503..48427895hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629791
Samples
Known GenesXYLT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032488
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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