A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790352



Internal ID21235690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:310177..319614hg38UCSC Ensembl
chr11:310177..319614hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389438
hg199438
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711015
SamplesCHM13
Known GenesIFITM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790352
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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