A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790932



Internal ID21236270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:223787..224002hg38UCSC Ensembl
chr11:223787..224002hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705235
Samples
Known GenesSIRT3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790932
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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