A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671163



Internal ID9590582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152306400..152307372hg38UCSC Ensembl
chr1:152278876..152279848hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6331052, essv6336292, essv6473189, essv5997841
SamplesNA19443, NA19445, NA19712, NA19463
Known GenesFLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671163
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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