A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892376



Internal ID19183196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66394571..66412192hg38UCSC Ensembl
Outerchr13:66394571..66412192hg38UCSC Ensembl
Innerchr13:66968703..66986324hg19UCSC Ensembl
Outerchr13:66968703..66986324hg19UCSC Ensembl
Innerchr13:65866704..65884325hg18UCSC Ensembl
Outerchr13:65866704..65884325hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3817622
hg1917622
hg1817622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783828
Samples
Known GenesPCDH9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892376
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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