A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797490



Internal ID19172212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67001434..67016946hg38UCSC Ensembl
Innerchr13:67575566..67591078hg19UCSC Ensembl
Innerchr13:66473567..66489079hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3815513
hg1915513
hg1815513
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892378
Supporting Variants
Samples
Known GenesPCDH9, PCDH9-AS4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797490
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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