A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671128



Internal ID9590547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106559391..106560705hg38UCSC Ensembl
Outerchr6:106559354..106560755hg38UCSC Ensembl
Innerchr6:107007266..107008580hg19UCSC Ensembl
Outerchr6:107007229..107008630hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6584326
SamplesNA19474
Known GenesAIM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671128
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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