A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11014099



Internal ID6010513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53012572..53013781hg38UCSC Ensembl
Innerchr3:53012572..53013781hg38UCSC Ensembl
Outerchr3:53012274..53014129hg38UCSC Ensembl
chr3:53046588..53047797hg19UCSC Ensembl
Innerchr3:53046588..53047797hg19UCSC Ensembl
Outerchr3:53046290..53048145hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596165
Supporting Variants
SamplesNA19428
Known GenesSFMBT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11014099
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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