A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669951



Internal ID9589370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28167428..28171202hg38UCSC Ensembl
chr10:28456357..28460131hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6261890
SamplesHG00556
Known GenesMPP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669951
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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