A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682736



Internal ID21204592
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 StatusS
Merged Variantsnsv2794360
Supporting Variants
Samples
Known GenesDAAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682736
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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