A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675273



Internal ID9941378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55606510..55612652hg38UCSC Ensembl
Outerchr6:55606353..55612805hg38UCSC Ensembl
Innerchr6:55471308..55477450hg19UCSC Ensembl
Outerchr6:55471151..55477603hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg386453
hg196453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1118e199
Supporting Variantsessv5830957
SamplesHG01051
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675273
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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