A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244941



Internal ID22049551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145757833..145757833hg38UCSC Ensembl
chr5:145137396..145137396hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244941
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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