A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9754554



Internal ID18382114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:324037..324098hg38UCSC Ensembl
chr19:324037..324098hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555807
Supporting Variants
Samples
Known GenesMIER2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9754554
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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