A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004909



Internal ID7070005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:169781776..169791951hg38UCSC Ensembl
Outerchr6:170181872..170192047hg19UCSC Ensembl
Outerchr6:169923797..169933972hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810176
hg1910176
hg1810176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564824
SamplesHuRef
Known GenesLINC00242, LINC00574
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004909
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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