A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247134



Internal ID22051744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61175774..61175774hg38UCSC Ensembl
chr10:62935532..62935532hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247134
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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