A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636292



Internal ID7023088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43598985..43609178hg38UCSC Ensembl
chr15:43891183..43901376hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3810194
hg1910194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231234, essv15231260, essv15231225, essv15231253, essv15231275, essv15231235, essv15231250, essv15231242, essv15231214, essv15231202, essv15231291, essv15231285, essv15231239, essv15231254, essv15231206, essv15231268, essv15231288, essv15231213, essv15231230, essv15231199, essv15231292, essv15231257, essv15231210, essv15231296, essv15231271, essv15231273, essv15231204, essv15231237, essv15231264, essv15231251, essv15231248, essv15231290, essv15231219, essv15231274, essv15231272, essv15231277, essv15231252, essv15231228, essv15231276, essv15231231, essv15231270, essv15231220, essv15231244, essv15231280, essv15231200, essv15231201, essv15231238, essv15231278, essv15231282, essv15231258, essv15231241, essv15231216, essv15231286, essv15231240, essv15231215, essv15231207, essv15231222, essv15231263, essv15231247, essv15231281, essv15231226, essv15231197, essv15231224, essv15231233, essv15231261, essv15231287, essv15231232, essv15231297, essv15231267, essv15231284, essv15231212, essv15231203, essv15231198, essv15231255, essv15231209, essv15231217, essv15231196, essv15231262, essv15231223, essv15231259, essv15231294, essv15231246, essv15231221, essv15231265, essv15231218, essv15231279, essv15231295, essv15231249, essv15231283, essv15231289, essv15231211, essv15231227, essv15231205, essv15231208, essv15231266, essv15231293, essv15231229, essv15231269, essv15231243, essv15231245, essv15231256, essv15231236
SamplesNA19394, HG04212, HG02614, HG02658, HG03857, HG02496, HG01462, HG03731, HG01031, HG03558, NA18639, HG03100, HG03229, HG02040, NA19098, NA18870, HG02769, HG03464, HG03436, HG02621, HG03706, HG02810, HG02407, NA20317, HG04070, HG03040, HG02922, HG02281, HG02562, NA19383, HG02315, HG03268, HG02736, HG03212, HG02471, NA19026, NA20845, HG02427, NA18864, HG03267, NA19025, NA18640, HG03114, HG03884, NA19921, HG02009, HG01353, NA12777, HG01183, HG02570, NA18934, HG01670, HG04146, HG01882, HG04162, HG00320, NA18910, NA18976, HG04180, HG02757, HG01047, HG03742, HG04054, NA11840, HG04155, HG03046, HG03006, HG04159, HG03109, HG02568, NA19035, NA20296, HG02613, HG01812, HG04025, NA18909, HG03461, NA20276, HG02010, NA19019, HG01974, NA19324, HG03019, HG04023, NA06994, NA18971, NA19438, NA19351, NA21102, NA19468, HG03279, NA20852, NA18873, HG03410, NA18876, HG03872, NA19213, NA20503, NA19030, HG03882, HG04056, HG00255
Known GenesCKMT1B, RNU6-28P, STRC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636292
Frequency
Sample Size2504
Observed Gain102
Observed Loss0
Observed Complex0
Frequencyn/a


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