A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819134



Internal ID21264472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134376628..134376628hg38UCSC Ensembl
chr9:137268474..137268474hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704842
Samples
Known GenesRXRA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819134
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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