A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244816



Internal ID22049426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128082732..128082732hg38UCSC Ensembl
chr5:127418424..127418424hg19UCSC Ensembl
Cytoband5q23.3
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 Variantsnssv17858234
Samples
Known GenesFLJ33630
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244816
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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