A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790379



Internal ID21235717
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 StatusM
Merged Variants
Supporting Variantsnssv13711295
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790379
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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