A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790377



Internal ID21235715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055105..36055105hg38UCSC Ensembl
chr11:36076655..36076655hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684697, nssv13683289
Samples
Known GenesLDLRAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790377
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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