A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765774



Internal ID20541634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129520497..129520497hg38UCSC Ensembl
chr10:131318761..131318761hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272928
Samples
Known GenesMGMT
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765774
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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