A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705167



Internal ID21226972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66376333..66376333hg38UCSC Ensembl
chr8:67288568..67288568hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705167
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.59375


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