A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603839



Internal ID6990870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2781085..2792635hg38UCSC Ensembl
Innerchr5:2781087..2792634hg38UCSC Ensembl
Outerchr5:2781084..2792637hg38UCSC Ensembl
chr5:2781199..2792749hg19UCSC Ensembl
Innerchr5:2781201..2792748hg19UCSC Ensembl
Outerchr5:2781198..2792751hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811551
hg1911551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11790311, essv11790312, essv11790310, essv11790313, essv11790314
SamplesHG04096, HG03874, HG03788, HG03991, NA21144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603839
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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