A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687132



Internal ID21208891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:131150..131150hg38UCSC Ensembl
chr11:186391..186391hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796606
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687132
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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