A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669392



Internal ID9935497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14970884..14976110hg38UCSC Ensembl
chr6:14971115..14976341hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6543841
SamplesNA19655
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669392
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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