A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683533



Internal ID21205388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86110824..86110824hg38UCSC Ensembl
chr11:85821866..85821866hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683533
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.5


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