A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695784



Internal ID21217638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1628738..1628738hg38UCSC Ensembl
chr19:1628737..1628737hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799415
Supporting Variants
Samples
Known GenesTCF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695784
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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