A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665603



Internal ID9931708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10894205..10896071hg38UCSC Ensembl
chr1:10954262..10956128hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6392155, essv5574397, essv6506565, essv6102736, essv6336021, essv6214075
SamplesHG01441, HG01188, HG00257, HG00640, HG00327, HG01047
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665603
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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