A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636466



Internal ID21828513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35934553..35934553hg38UCSC Ensembl
chr17:34261557..34261557hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090924
Supporting Variants
Samples
Known GenesLYZL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636466
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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