A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575173



Internal ID21767216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108989527..108989527hg38UCSC Ensembl
chr6:109310730..109310730hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063318
Supporting Variants
Samples
Known GenesSESN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17575173
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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