A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1001897



Internal ID7067015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:147314354..147315244hg38UCSC Ensembl
Innerchr7:147011446..147012336hg19UCSC Ensembl
Innerchr7:146642379..146643269hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38891
hg19891
hg18891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv177e180
Supporting Variantsessv3587069
SamplesHuRef
Known GenesCNTNAP2, MIR548I4
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1001897
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