A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17860225



Internal ID22043868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23539549..23539549hg38UCSC Ensembl
chr7:23579168..23579168hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6261184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17860225
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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