A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848656



Internal ID22032299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73968930..73968930hg38UCSC Ensembl
chr15:74261271..74261271hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249827
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848656
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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