A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681303



Internal ID21203167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36497148..36497148hg38UCSC Ensembl
chr21:37869446..37869446hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804074
Supporting Variants
Samples
Known GenesCLDN14
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681303
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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