A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676168



Internal ID9595587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28574150..28575896hg38UCSC Ensembl
Outerchr1:28574113..28575946hg38UCSC Ensembl
Innerchr1:28900662..28902408hg19UCSC Ensembl
Outerchr1:28900625..28902458hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381834
hg191834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34e199
Supporting Variantsessv5715736
SamplesHG00701
Known GenesTRNAU1AP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676168
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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