A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6248478



Internal ID22053088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96711176..96711176hg38UCSC Ensembl
chr12:97104954..97104954hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17843987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6248478
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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