A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241057



Internal ID22045667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56352349..56352349hg38UCSC Ensembl
chr12:56746133..56746133hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17844292
Samples
Known GenesSTAT2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241057
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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