A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699791



Internal ID21221633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158440322..158440322hg38UCSC Ensembl
chr5:157867330..157867330hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg384939
hg194939
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699791
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.1875


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