A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14777470



Internal ID4779286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66317472..66327540hg38UCSC Ensembl
chr13:66891604..66901672hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3810069
hg1910069
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632503
Supporting Variants
SamplesHG03130
Known GenesPCDH9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14777470
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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