A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242070



Internal ID22046680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51930068..51930068hg38UCSC Ensembl
chr15:52222265..52222265hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242070
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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