A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665730



Internal ID9585150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6374440..6385243hg38UCSC Ensembl
Outerchr1:6374403..6385293hg38UCSC Ensembl
Innerchr1:6434500..6445303hg19UCSC Ensembl
Outerchr1:6434463..6445353hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3810891
hg1910891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11e199
Supporting Variantsessv5540377
SamplesHG00684
Known GenesACOT7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665730
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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