A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698185



Internal ID21220039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45643101..45643101hg38UCSC Ensembl
chr6:45610838..45610838hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698185
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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