A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846527



Internal ID22030170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91190352..91190352hg38UCSC Ensembl
chr15:91733582..91733582hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249942
Supporting Variants
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846527
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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