A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674800



Internal ID9940905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36625907..36633271hg38UCSC Ensembl
chr11:36647457..36654821hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387365
hg197365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6322904, essv6405687, essv5624653, essv6078047, essv6107245, essv5972983, essv5995006, essv5634990, essv5429424, essv5470199, essv5494061, essv5761540, essv5800671, essv6581880, essv5868129, essv6026952, essv5430270, essv5547306, essv6094554, essv5774060, essv6467643, essv6269238, essv6180775
SamplesNA19350, NA19819, NA20332, NA18510, NA18519, NA18923, NA19138, NA18874, NA19921, HG01124, NA18907, NA19449, NA19099, NA19225, NA18523, NA19834, NA19712, NA19473, NA19398, NA19713, NA19213, NA19900, NA19316
Known GenesC11orf74
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674800
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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