A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672033



Internal ID9938138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3574732..3583882hg38UCSC Ensembl
Outerchr6:3574695..3583932hg38UCSC Ensembl
Innerchr6:3574966..3584116hg19UCSC Ensembl
Outerchr6:3574929..3584166hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg389238
hg199238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5765680
SamplesNA18609
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672033
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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