A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184471



Internal ID21323276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9058020..9058020hg38UCSC Ensembl
chr18:9058018..9058018hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948676
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184471
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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