A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665113



Internal ID9584532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162162737..162165776hg38UCSC Ensembl
chr6:162583769..162586808hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383040
hg193040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1167e199
Supporting Variantsessv6069823, essv6001899, essv5693831, essv5606231, essv6253391, essv5755517, essv5899801, essv6044867, essv5499795, essv6567183, essv6392100, essv5691770, essv5840938, essv5674833, essv5670771, essv6345024, essv5498917, essv5964056, essv6325765, essv5497764, essv6553270, essv5768967, essv5435122, essv5791989, essv6022269, essv6399705, essv5861299, essv5942835, essv5645564, essv5494091, essv5965474, essv6217532, essv5623533, essv5795377, essv6544879, essv6275319, essv5805302, essv5737042, essv5925390, essv5694236, essv6562158, essv6146168, essv6577791, essv6453525, essv5836089, essv5766593, essv6106618, essv6475979, essv6024902, essv5588422, essv5484806, essv6211691, essv5402105, essv5575229, essv5879100, essv5840535, essv6274319, essv5900913, essv6003442, essv6533343, essv6012733, essv5469185, essv5693059, essv6536824, essv6435340, essv6177802, essv5886127, essv5601680, essv5399537, essv6394178, essv5716740, essv5572423, essv6352488, essv5741073, essv6485548, essv5444828, essv5688424, essv6156434, essv6147355, essv6412487, essv5477607, essv6513938, essv5796665, essv5529038, essv6018869, essv6305135, essv6571683, essv5980761, essv5774116, essv5545765, essv6221659, essv5410079, essv6400308, essv5494912, essv5511337, essv6369024, essv5745341, essv6365778, essv5565499, essv5758196, essv6349074, essv6229967, essv5551115, essv5561543, essv6412141
SamplesHG00096, HG00189, NA19648, HG00143, NA19397, NA19466, NA11829, NA19399, NA19332, HG01079, NA11920, NA20294, NA19355, NA19393, HG00566, NA19377, HG00737, HG01461, NA19443, HG01051, NA18633, NA12155, NA12341, HG01250, NA19396, NA19381, NA19373, NA19379, HG01366, NA19448, NA19678, NA20774, NA20317, NA19916, HG00330, HG01365, HG00334, NA19782, NA19384, NA19079, NA19720, NA19383, NA20819, HG00232, NA19372, NA19371, NA19471, HG01440, NA19189, HG01048, HG01133, HG00253, NA19921, HG01124, HG00133, HG01136, HG00188, NA19908, NA19247, HG00268, HG01384, NA19403, NA20809, NA19455, NA19236, NA19982, NA12718, NA18910, HG00690, HG00404, HG01197, NA19453, NA19338, NA19395, NA20534, NA19440, NA19390, NA18909, NA19434, HG00366, NA19473, HG00136, NA19435, NA19444, HG00278, NA20792, NA19428, NA20544, HG00319, HG01108, NA12347, NA19398, NA18631, NA19438, NA19468, HG00280, NA19213, NA19661, NA19430, NA19755, NA18511, NA18612, NA19429, HG01437, NA19431
Known GenesPARK2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665113
Frequency
Sample Size1151
Observed Gain0
Observed Loss105
Observed Complex0
Frequencyn/a


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