A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667130



Internal ID9586549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35360336..35372805hg38UCSC Ensembl
chr19:35851238..35863707hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812470
hg1912470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv637e199
Supporting Variantsessv5663261, essv5772009, essv6424000, essv6224004, essv6550807, essv6494115, essv6124324, essv5768872, essv6430212, essv5721373, essv6203926, essv5397683, essv6165539, essv5976783, essv6229528, essv6312351, essv5815071, essv6527510, essv5960479, essv6095450, essv6021538, essv5945458, essv5432472, essv6307362, essv6341877, essv5612090, essv6433426, essv6017759, essv6414381, essv6063714, essv6258309, essv6010584, essv5714487, essv6240486, essv6003268, essv5411487, essv5974966, essv6104304, essv6193732, essv6089873, essv6082176, essv6405923, essv5804772, essv5633416, essv6496950, essv5608840, essv5575289, essv5501167, essv5435849, essv5863569
SamplesHG00096, HG00114, HG01441, HG01356, HG00231, HG00249, HG00257, HG01389, HG00244, HG01465, HG01456, HG00127, HG01350, HG00247, HG01365, HG00158, HG00139, HG00148, HG00106, HG00236, HG01495, HG00262, HG00232, HG01440, HG00160, HG00118, HG00253, HG00264, HG00108, HG00137, HG00154, HG01498, HG00263, HG00239, HG00146, HG00126, HG00258, HG00155, HG00254, HG00119, HG01253, HG00136, HG00237, HG01342, HG00259, HG00112, HG00252, HG01377, HG01125, HG01112
Known GenesFFAR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667130
Frequency
Sample Size1151
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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