A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854536



Internal ID22038179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87892607..87892607hg38UCSC Ensembl
chr4:88813759..88813759hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6254954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854536
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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