A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702630



Internal ID21224451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111895709..111895709hg38UCSC Ensembl
chr8:112907938..112907938hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702630
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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