A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676531



Internal ID21233442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15113148..15113148hg38UCSC Ensembl
chr11:15134694..15134694hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790302
Supporting Variants
Samples
Known GenesINSC
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676531
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.53125


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