A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15204406



Internal ID21343206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28267076..28267076hg38UCSC Ensembl
chr8:28124593..28124593hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926793
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15204406
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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