A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636291



Internal ID7023087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43598985..43609178hg38UCSC Ensembl
chr15:43891183..43901376hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3810194
hg1910194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231157, essv15231175, essv15231189, essv15231159, essv15231158, essv15231156, essv15231162, essv15231176, essv15231180, essv15231192, essv15231187, essv15231153, essv15231167, essv15231182, essv15231163, essv15231177, essv15231178, essv15231173, essv15231194, essv15231165, essv15231160, essv15231174, essv15231171, essv15231161, essv15231181, essv15231166, essv15231191, essv15231164, essv15231190, essv15231188, essv15231168, essv15231193, essv15231179, essv15231184, essv15231195, essv15231154, essv15231186, essv15231170, essv15231185, essv15231169, essv15231183, essv15231155, essv15231172
SamplesHG00189, HG02628, HG00102, NA11920, HG03057, HG02275, HG03518, NA20359, HG01350, HG00589, NA11992, NA18498, HG01628, NA19238, HG01284, HG00160, HG00530, NA18638, HG02047, HG01248, NA18538, HG01149, HG03919, HG00284, NA20903, NA19449, HG02445, HG03388, HG00117, NA18963, NA18536, NA20801, NA12716, HG03790, HG00638, NA20362, HG03846, HG04090, HG03419, HG00478, HG03077, HG03886, NA20511
Known GenesCKMT1B, RNU6-28P, STRC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636291
Frequency
Sample Size2504
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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