A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248486



Internal ID22053096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97268741..97268741hg38UCSC Ensembl
chr12:97662519..97662519hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248486
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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