A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584604



Internal ID21776647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104345830..104345830hg38UCSC Ensembl
chr8:105358058..105358058hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074746
Supporting Variants
Samples
Known GenesDCSTAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584604
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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