A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7388913



Internal ID10667195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:65866018..65866362hg38UCSC Ensembl
Outerchr18:63533254..63533598hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3119346
Supporting Variants
SamplesHuRef
Known GenesCDH7
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7388913
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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