A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678166



Internal ID21200029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8737990..8737990hg38UCSC Ensembl
chr16:8831847..8831847hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795646
Supporting Variants
Samples
Known GenesABAT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678166
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.758621


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