A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672901



Internal ID9939006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2791329..2809985hg38UCSC Ensembl
chr6:2791563..2810219hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3818657
hg1918657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5444308, essv5955495
SamplesHG01359, HG00554
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672901
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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