A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666560



Internal ID9932665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24861885..24864274hg38UCSC Ensembl
chr15:25107032..25109421hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382390
hg192390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6193957, essv5511082, essv5559105, essv5727818, essv6320564, essv5499096, essv5968938, essv6356481, essv5638962, essv5566607, essv5947834, essv5707311, essv5935604, essv6591485, essv5909914, essv5878514, essv6394580, essv6049407, essv6498690, essv6500189, essv6401880, essv5814453, essv6273774, essv6065312, essv5549660, essv5766098, essv5460355, essv5419503, essv5782872, essv5804231, essv5630390, essv5711288, essv5858197, essv6507239, essv6349705, essv6510870, essv6485881, essv5578485, essv5446591, essv6526983, essv6381689, essv5461303, essv6564868, essv6290820, essv5812156, essv6264538, essv6006641, essv5435591, essv6556900, essv6095628, essv6374638, essv5743532, essv6508856, essv6210564, essv6350807, essv5854538, essv6246903, essv5808135, essv5617067, essv6227933
SamplesNA18502, NA19466, NA18508, NA18980, HG01188, NA18603, NA19355, NA18870, HG01051, NA18510, NA19381, NA18940, NA18519, HG00689, NA19131, NA19197, NA19313, NA18498, NA20278, NA18874, NA18868, NA19917, NA19137, NA19372, HG00422, NA19189, NA20342, NA18908, NA18867, HG00543, NA19247, NA18538, NA19347, NA18933, NA19982, HG00533, NA18912, NA18523, NA19160, NA19625, NA18858, NA19436, NA18533, NA19390, NA18535, NA19147, NA18517, HG00565, HG00638, NA19331, NA19144, NA19334, HG01108, HG00662, NA20348, HG00186, NA19116, NA19129, NA19004, NA18549
Known GenesSNRPN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666560
Frequency
Sample Size1151
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


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