A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1790143



Internal ID12606575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152229137..152229225hg38UCSC Ensembl
chr3:151946926..151947014hg19UCSC Ensembl
chr3:153429616..153429704hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3889
hg1989
hg1889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3980312
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1790143
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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