A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6245292



Internal ID22049902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156136117..156136117hg38UCSC Ensembl
chr1:156105908..156105908hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860142
Samples
Known GenesLMNA, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6245292
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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