A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2808570



Internal ID21253908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174320515..174320515hg38UCSC Ensembl
chr4:175241666..175241666hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382638
hg192638
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693990
Samples
Known GenesCEP44
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2808570
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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