A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242002



Internal ID22046612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44346324..44346324hg38UCSC Ensembl
chr15:44638522..44638522hg19UCSC Ensembl
Cytoband15q15.3
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 Variantsnssv17846442
Samples
Known GenesCASC4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242002
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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