A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672582



Internal ID9938687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121010188..121027998hg38UCSC Ensembl
chr10:122769701..122787511hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3817811
hg1917811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171e199
Supporting Variantsessv5521653, essv6447935, essv5825167, essv6092586, essv5428535, essv5652941, essv5560161, essv6089836, essv6459252, essv6512646, essv6559928, essv6196125, essv5783159, essv6344302, essv6467029, essv5796912, essv6137596, essv5561811, essv5937068, essv6298904, essv5487107, essv6563522, essv6034821, essv6102394, essv6463468
SamplesNA19394, NA19359, NA19379, NA19317, NA19901, NA19189, NA20342, NA20127, NA18867, NA19451, NA19707, NA19403, NA18933, NA19391, NA19327, HG01101, NA18853, NA20282, NA19452, NA19318, NA19256, NA19712, NA19444, NA20281, NA19818
Known GenesMIR5694
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672582
Frequency
Sample Size1151
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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