A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13690168



Internal ID21212020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103909377..103909377hg38UCSC Ensembl
chr10:105669135..105669135hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789059
Supporting Variants
Samples
Known GenesOBFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13690168
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.359375


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