A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671514



Internal ID9937619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26961176..26961571hg38UCSC Ensembl
chr1:27287667..27288062hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6426336, essv6594541, essv6248633, essv6188587, essv6498050, essv6405738, essv6371698, essv6330238, essv5693358, essv6286697, essv6188311, essv6071216, essv6487371, essv6126844, essv5506767, essv5633661, essv6530760, essv5935073, essv6142312, essv5636100, essv6312555, essv5486119, essv6084185, essv5827975, essv6041653, essv6127615, essv6317538, essv6050516, essv5806053, essv5680263, essv6055621, essv6541642, essv5996080, essv5812587, essv6341931, essv5797781, essv6094520, essv5674645, essv6207800, essv6152808, essv5545135, essv6338259, essv5459836, essv6509461, essv6548667, essv6042012, essv6108865, essv5623078, essv5495486, essv5860587, essv5426638, essv6376934, essv6572899, essv5922137, essv6390557, essv6100320, essv5867432, essv5997698, essv5882293, essv5911882, essv6578635, essv5626743, essv6283118, essv5559363, essv5799790, essv6531659, essv5708963, essv5418416, essv6174480, essv6597925
SamplesNA18502, NA19909, NA18947, NA19466, NA19204, NA18508, NA19399, NA18507, HG00640, NA19350, NA19359, NA19092, NA18486, NA12751, NA19355, NA19393, NA18967, HG00641, NA19373, NA19171, NA18519, HG01070, NA19201, NA18960, NA19197, HG01083, NA18498, NA19384, NA19404, HG01067, NA19137, NA19372, NA19385, NA19172, NA19159, HG01048, NA19209, NA19456, NA18908, NA19921, NA11831, NA19908, NA19403, NA19152, NA18956, NA18516, NA19982, NA18981, NA19114, NA19449, NA19453, NA20282, NA19761, NA19395, NA18858, NA18542, NA18909, NA18517, NA19144, NA19439, NA19376, NA19328, NA18971, NA19223, NA19093, NA19116, NA19900, HG01125, NA18522, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671514
Frequency
Sample Size1151
Observed Gain0
Observed Loss70
Observed Complex0
Frequencyn/a


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