A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249943



Internal ID22054553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91294584..91294584hg38UCSC Ensembl
chr15:91837814..91837814hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846528
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249943
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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