A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17857187



Internal ID22040830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43939076..43939076hg38UCSC Ensembl
chr5:43939178..43939178hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6260269
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17857187
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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