A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809945



Internal ID21255283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94043583..94043583hg38UCSC Ensembl
chr3:93762427..93762427hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691579
Samples
Known GenesARL13B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809945
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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