A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667926



Internal ID9934031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107364990..107373196hg38UCSC Ensembl
Outerchr11:107364519..107373716hg38UCSC Ensembl
Innerchr11:107235716..107243922hg19UCSC Ensembl
Outerchr11:107235245..107244442hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg389198
hg199198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv239e199
Supporting Variantsessv5701081, essv6162471, essv5565052, essv5447763, essv6383351, essv5929532, essv5473422, essv5798755, essv5606693, essv6358527, essv6150060, essv6363808, essv6159197, essv6377312, essv5646911, essv5434979, essv6039995, essv6344761, essv5554257, essv6175880, essv6507714, essv6167428, essv6188512, essv6303328, essv5707888, essv5520936, essv6113969, essv6275529, essv6296908, essv6556503, essv5813649, essv6527255, essv6590308, essv6025557, essv6396053, essv5482077, essv6483830, essv6293723, essv6221365, essv5987584, essv6257014, essv5660103, essv6396193, essv5550979, essv5562863, essv5877583, essv5591661, essv6185184, essv6332336, essv6551303, essv5890301, essv5943617, essv6304682, essv6246696, essv5773561, essv6562541, essv5716130, essv5668983, essv6503126, essv5964739, essv5886496
SamplesNA11830, NA12286, NA11995, NA12273, NA18980, NA12843, NA11933, NA11931, NA12045, NA12751, NA19057, NA18959, NA12399, NA12155, NA19067, NA12341, NA19076, NA19005, NA18982, NA19062, NA11992, NA07048, NA12283, NA19054, NA18949, NA11932, NA11994, NA18986, NA18990, NA12828, NA18975, NA18973, NA11993, NA12777, NA18951, NA19056, NA12342, NA19081, NA19064, NA12249, NA06989, NA19059, NA18963, NA12546, NA12043, NA18953, NA12716, NA18952, NA19010, NA12046, NA18943, NA12763, NA19085, NA18971, NA18987, NA18972, NA18983, NA18989, NA12890, NA19065, NA11832
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667926
Frequency
Sample Size1151
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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