A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1468878



Internal ID12632000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25248030..25248030hg38UCSC Ensembl
chr20:25228666..25228666hg19UCSC Ensembl
chr20:25176666..25176666hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4090096
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1468878
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer