A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705268



Internal ID21227072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102867904..102867904hg38UCSC Ensembl
chr8:103880132..103880132hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705268
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.359375


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