A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685706



Internal ID21207565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18832968..18832968hg38UCSC Ensembl
chr20:18813612..18813612hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685706
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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