A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677328



Internal ID21199180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40881051..40881051hg38UCSC Ensembl
chr19:41386956..41386956hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386169
hg196169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800016
Supporting Variants
Samples
Known GenesCYP2A7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677328
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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