A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038252



Internal ID21947595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35930228..35958671hg38UCSC Ensembl
chr17:34257232..34285675hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3828444
hg1928444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622240
Samples
Known GenesLYZL6, RDM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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