A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259849



Internal ID22064459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156835892..156835892hg38UCSC Ensembl
chr3:156553681..156553681hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17854221
Samples
Known GenesLEKR1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259849
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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