A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761553



Internal ID18735799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160962740..160967712hg38UCSC Ensembl
Outerchr3:160962213..160968299hg38UCSC Ensembl
Innerchr3:160680528..160685500hg19UCSC Ensembl
Outerchr3:160680001..160686087hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg386087
hg196087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562806
Supporting Variants
Samples
Known GenesPPM1L
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761553
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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