A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799415



Internal ID21244753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1628738..1628738hg38UCSC Ensembl
chr19:1628737..1628737hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695784, nssv13678120
Samples
Known GenesTCF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799415
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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