A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679685



Internal ID21201543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50666189..50666189hg38UCSC Ensembl
chr20:49282726..49282726hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802904
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679685
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.706897


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