A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660639



Internal ID9926744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9359324..9360128hg38UCSC Ensembl
Outerchr6:9359287..9360178hg38UCSC Ensembl
Innerchr6:9359557..9360361hg19UCSC Ensembl
Outerchr6:9359520..9360411hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5600594
SamplesNA18602
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660639
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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