A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711295



Internal ID21233056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36145335..36145461hg38UCSC Ensembl
chr11:36166885..36167011hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790379
Supporting Variants
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711295
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.65625


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