A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642628



Internal ID21590933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129520507..129520507hg38UCSC Ensembl
chr10:131318771..131318771hg19UCSC 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 Variantsnssv17066814
SamplesHG00731
Known GenesMGMT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642628
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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