A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558651



Internal ID21883006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132792356..132792356hg38UCSC Ensembl
chr6:133113495..133113495hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061506
Supporting Variants
Samples
Known GenesSLC18B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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