A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699448



Internal ID21221289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:26643837..26643837hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699448
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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