A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699840



Internal ID21221676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169242814..169242814hg38UCSC Ensembl
chr6:169642909..169642909hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813617
Supporting Variants
Samples
Known GenesTHBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699840
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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