A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580718



Internal ID21772761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129520507..129520507hg38UCSC Ensembl
chr10:131318771..131318771hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097845
Supporting Variants
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580718
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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