A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626632



Internal ID6666782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63272529..63273630hg38UCSC Ensembl
Innerchr11:63272530..63273630hg38UCSC Ensembl
Outerchr11:63272529..63273631hg38UCSC Ensembl
chr11:63040001..63041102hg19UCSC Ensembl
Innerchr11:63040002..63041102hg19UCSC Ensembl
Outerchr11:63040001..63041103hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14182337, essv14182346, essv14182321, essv14182350, essv14182334, essv14182332, essv14182338, essv14182355, essv14182319, essv14182359, essv14182318, essv14182328, essv14182343, essv14182335, essv14182339, essv14182349, essv14182351, essv14182326, essv14182356, essv14182324, essv14182342, essv14182361, essv14182336, essv14182357, essv14182348, essv14182341, essv14182353, essv14182320, essv14182322, essv14182316, essv14182333, essv14182360, essv14182345, essv14182331, essv14182344, essv14182362, essv14182352, essv14182325, essv14182347, essv14182327, essv14182358, essv14182323, essv14182329, essv14182317, essv14182363, essv14182330, essv14182354, essv14182340
SamplesHG02339, NA19700, NA19909, HG03163, NA19092, HG03280, NA19819, HG03372, HG03478, HG01366, NA19197, HG03520, NA18874, NA19372, NA19385, HG02427, NA19027, HG02479, HG02570, NA19347, NA19984, HG03457, HG02953, HG02497, HG03311, HG02429, NA20299, NA19042, NA18856, HG03451, HG03354, NA19160, NA19095, NA19625, NA19206, HG03469, HG02464, NA19360, HG03112, HG03157, HG02938, NA19474, HG03410, HG01883, NA19030, HG03162, NA19346, HG03196
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626632
Frequency
Sample Size2504
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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