A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674931



Internal ID9941036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63068993..63076819hg38UCSC Ensembl
chr11:62836465..62844291hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387827
hg197827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5713335, essv6337978, essv5764974, essv6107693, essv5555789, essv6565241, essv5680378, essv5873321, essv5473179, essv6272105
SamplesNA19700, NA19819, NA18504, HG01366, NA18874, NA19371, NA19347, NA18856, NA19311, NA19360
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674931
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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