A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794650



Internal ID21239988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86410878..86410878hg38UCSC Ensembl
chr15:86954109..86954109hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13676857
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794650
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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