A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795382



Internal ID21240720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80288307..80288307hg38UCSC Ensembl
chr15:80580649..80580649hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13694061
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795382
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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