A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683501



Internal ID21205366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94043558..94043558hg38UCSC Ensembl
chr3:93762402..93762402hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808036
Supporting Variants
Samples
Known GenesARL13B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683501
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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