A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3550237



Internal ID18404627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28377409..28377475hg38UCSC Ensembl
chr13:28951546..28951612hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9748984
Samples
Known GenesFLT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3550237
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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