A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9748981



Internal ID18723227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28065608..28065797hg38UCSC Ensembl
Outerchr13:28065603..28065815hg38UCSC Ensembl
Innerchr13:28639745..28639934hg19UCSC Ensembl
Outerchr13:28639740..28639952hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550234
Supporting Variants
Samples
Known GenesFLT3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9748981
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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