A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809239



Internal ID21254577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109864518..109864518hg38UCSC Ensembl
chr4:110785674..110785674hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688650
Samples
Known GenesLRIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809239
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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