A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256186



Internal ID22060796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32762472..32762472hg38UCSC Ensembl
chr5:32762578..32762578hg19UCSC Ensembl
Cytoband5p13.3
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 Variantsnssv17856950
Samples
Known GenesNPR3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256186
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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