A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857786



Internal ID22041429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92413759..92413759hg38UCSC Ensembl
chr5:91749466..91749466hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6244538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857786
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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