A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv930499



Internal ID17307827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:77755038..77755075hg38UCSC Ensembl
Outerchr16:77788935..77788972hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1607690
Samples
Known Genes
MethodSequencing
Analysis
PlatformNot reported
CommentsretroCNV insertion of a retrotransposition of MIER1 mRNA.
ReferenceSchrider_et_al_2013
Pubmed ID23359205
Accession Number(s)nsv930499
Frequency
Sample Size946
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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