A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794660



Internal ID21239998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871539..90871539hg38UCSC Ensembl
chr15:91414769..91414769hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701538
Samples
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794660
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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