A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756606



Internal ID20532466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169485876..169485876hg38UCSC Ensembl
chr3:169203664..169203664hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264409
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756606
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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