A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789126



Internal ID21234464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129520529..129520529hg38UCSC Ensembl
chr10:131318793..131318793hg19UCSC 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 Variantsnssv13681010
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789126
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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