A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438911



Internal ID22496781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106339520..106339520hg38UCSC Ensembl
chr8:107351748..107351748hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952712
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438911
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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