A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683663



Internal ID21205521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121786124..121786124hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683663
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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