A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676330



Internal ID9942435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63219932..63238966hg38UCSC Ensembl
Outerchr6:63219884..63239022hg38UCSC Ensembl
Innerchr6:63929837..63948871hg19UCSC Ensembl
Outerchr6:63929789..63948927hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3819139
hg1919139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5722057
SamplesNA19311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676330
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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