A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3791259



Internal ID11970612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:381388..381580hg38UCSC Ensembl
chr11:381388..381580hg19UCSC Ensembl
chr11:371388..371580hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38193
hg19193
hg18193
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1612736
Supporting Variants
SamplesHuRef
Known GenesB4GALNT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3791259
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