A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678865



Internal ID9598284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11928601..11935157hg38UCSC Ensembl
Outerchr19:11928230..11935777hg38UCSC Ensembl
Innerchr19:12039416..12045972hg19UCSC Ensembl
Outerchr19:12039045..12046592hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv623e199
Supporting Variantsessv5890407, essv5934731, essv6574127, essv6045430, essv5933057, essv5885738, essv5611696, essv6152797, essv5505986, essv6131467, essv6499755, essv6160651, essv6135346, essv6381230, essv6038014, essv5931063, essv5852892, essv5527104, essv6090675, essv6453123, essv5635604, essv5548629, essv6373926, essv5888927, essv5978271, essv5515879, essv5974801, essv5515494, essv6262133, essv6226087, essv5739337, essv5612483, essv5555122, essv6347348, essv6059953, essv6568275, essv5469700, essv6194108, essv5892355, essv5743767, essv5481491, essv5525507, essv5777646, essv5670077, essv6261300, essv5468705, essv5863729, essv6056179, essv5505115, essv5539176, essv5821337, essv6130805, essv6378060, essv6130634, essv6304402, essv6043128, essv5573895, essv6557840, essv6315066, essv5902496, essv5542082, essv5710282, essv5869169, essv6051441, essv5545779, essv6402773, essv5967230, essv5549967, essv5458292, essv6456879, essv5452245, essv5614427, essv6062374, essv6342842, essv5961829, essv5620026, essv5547536, essv6281853, essv5789697, essv6585971, essv6155436, essv6329108, essv5476053, essv6321273, essv6336376
SamplesNA19207, NA18870, NA19248, NA19445, NA18520, NA19321, NA18933, NA19404, NA19437, NA19114, NA18874, NA19093, NA19223, NA19455, NA19319, NA19430, NA18516, NA19317, NA19334, NA19451, NA18517, NA18489, NA19461, NA19257, NA19108, NA19355, NA19472, NA19467, NA19147, NA19438, NA19463, NA19428, NA19383, NA18934, NA19390, NA18856, NA19429, NA19256, NA18916, NA19457, NA19324, NA19247, NA19360, NA19313, NA19129, NA19172, NA19189, NA19372, NA19393, NA19373, NA19384, NA18923, NA19102, NA18522, NA18502, NA19119, NA19098, NA18858, NA19347, NA19332, NA19131, NA19159, NA18910, NA19235, NA19376, NA18907, NA19391, NA19394, NA19403, NA19116, NA19434, NA19099, NA19446, NA19225, NA19160, NA19371, NA19198, NA19470, NA19315, NA19346, NA18853, NA19473, NA19468, NA19456, NA19466
Known GenesZNF700
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678865
Frequency
Sample Size1151
Observed Gain0
Observed Loss85
Observed Complex0
Frequencyn/a


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