A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241909



Internal ID22046519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8063985..8063985hg38UCSC Ensembl
chr2:8204115..8204115hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847931
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241909
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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