A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679944



Internal ID21201804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31689270..31689270hg38UCSC Ensembl
chr20:30277073..30277073hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802532
Supporting Variants
Samples
Known GenesBCL2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679944
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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