A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819054



Internal ID21264392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120667501..120667501hg38UCSC Ensembl
chr9:123429779..123429779hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702399
Samples
Known GenesMEGF9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819054
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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