A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701538



Internal ID21223363
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 StatusS
Merged Variantsnsv2794660
Supporting Variants
Samples
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701538
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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