A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676565



Internal ID21233477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91547397..91547397hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3895
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808891
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676565
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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