A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1668868



Internal ID12831987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52465512..52465610hg38UCSC Ensembl
chr4:53331678..53331776hg19UCSC Ensembl
chr4:53026435..53026533hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3876724
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1668868
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