A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1575834



Internal ID12738956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165293795..165294038hg38UCSC Ensembl
chr3:165011583..165011826hg19UCSC Ensembl
chr3:166494277..166494520hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38244
hg19244
hg18244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3925568
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1575834
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