A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558016



Internal ID21882371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25867127..25867127hg38UCSC Ensembl
chr6:25867355..25867355hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6062625
Supporting Variants
Samples
Known GenesSLC17A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558016
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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