A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664714



Internal ID9930819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28356959..28389265hg38UCSC Ensembl
Outerchr5:28356588..28389635hg38UCSC Ensembl
Innerchr5:28357066..28389372hg19UCSC Ensembl
Outerchr5:28356695..28389742hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3833048
hg1933048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5516108, essv6121039, essv6474675, essv6219305, essv6148389, essv6047428
SamplesNA19067, NA19062, NA19009, NA19060, NA18984, NA19004
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664714
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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