A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244012



Internal ID22048622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41754159..41754159hg38UCSC Ensembl
chr4:41756176..41756176hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244012
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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