A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794360



Internal ID21239698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59364971..59364971hg38UCSC Ensembl
chr14:59831689..59831689hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682736
Samples
Known GenesDAAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794360
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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