A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671556



Internal ID9937661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87816..202022hg38UCSC Ensembl
Outerchr6:87445..202392hg38UCSC Ensembl
Innerchr6:87816..202022hg19UCSC Ensembl
Outerchr6:87445..202392hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38114948
hg19114948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1068e199
Supporting Variantsessv5499770, essv5446187, essv5420715, essv6301235, essv6156202, essv6527045
SamplesHG01521, HG01518, HG01522, HG01519, HG01515, HG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671556
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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