A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2816861



Internal ID21262199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106285865..106285865hg38UCSC Ensembl
chr8:107298093..107298093hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697083
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2816861
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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