A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6258539



Internal ID22063149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1119211..1119211hg38UCSC Ensembl
chr12:1228377..1228377hg19UCSC Ensembl
Cytoband12p13.33
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 Variantsnssv17843134
Samples
Known GenesERC1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6258539
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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