A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666765



Internal ID9586184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28574439..28575944hg38UCSC Ensembl
Outerchr1:28574282..28576097hg38UCSC Ensembl
Innerchr1:28900951..28902456hg19UCSC Ensembl
Outerchr1:28900794..28902609hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381816
hg191816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34e199
Supporting Variantsessv6557015
SamplesHG00701
Known GenesTRNAU1AP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666765
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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