A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695286



Internal ID21217135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19860117..19860117hg38UCSC Ensembl
chr11:19881663..19881663hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789965
Supporting Variants
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695286
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.788462


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