A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671570



Internal ID9937675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28131516..28131855hg38UCSC Ensembl
Outerchr1:28131341..28132023hg38UCSC Ensembl
Innerchr1:28458027..28458366hg19UCSC Ensembl
Outerchr1:28457852..28458534hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6521150, essv6279414, essv6265668
SamplesHG01072, HG00732, HG01055
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671570
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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