A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17849034



Internal ID22032677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6549936..6549936hg38UCSC Ensembl
chr18:6549935..6549935hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6259181
Supporting Variants
Samples
Known GenesC18orf64
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17849034
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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