A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698331



Internal ID21220180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126358035..126358035hg38UCSC Ensembl
chr8:127370280..127370280hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698331
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.328125


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