A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259957



Internal ID22064567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169427212..169427212hg38UCSC Ensembl
chr3:169145000..169145000hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855004
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259957
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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