A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249122



Internal ID22053732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58325743..58325743hg38UCSC Ensembl
chr13:58899877..58899877hg19UCSC Ensembl
Cytoband13q21.1
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 Variantsnssv17844774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249122
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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