A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2811589



Internal ID21256928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176371499..176371499hg38UCSC Ensembl
chr5:175798502..175798502hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700556
Samples
Known GenesARL10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2811589
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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