A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3942716



Internal ID21362785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129520528..129520528hg38UCSC Ensembl
chr10:131318792..131318792hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191284
SamplesHG002
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3942716
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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