A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1166784



Internal ID11983221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45485378..45485509hg38UCSC Ensembl
chr13:46059513..46059644hg19UCSC Ensembl
chr13:44957514..44957645hg18UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38132
hg19132
hg18132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3779392
SamplesHuRef
Known GenesCOG3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1166784
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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