A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665175



Internal ID9931280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81866417..81866675hg38UCSC Ensembl
Outerchr16:81866380..81866725hg38UCSC Ensembl
Innerchr16:81900022..81900280hg19UCSC Ensembl
Outerchr16:81899985..81900330hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5797419, essv5464840, essv6565140, essv5580641, essv5823886, essv5734664, essv5871178, essv6505199, essv5721038, essv5613753, essv5588690, essv5606986, essv6548778, essv6530036, essv6250521, essv5880674, essv5909613, essv5881946, essv6238835, essv5553215, essv6177644, essv6542595, essv6174016, essv5867664, essv5663848, essv6038683, essv6304226, essv5898572, essv5481695, essv5824189, essv6538934, essv6430721, essv5590612, essv5480041, essv6403258, essv5908458, essv5982722, essv5431954, essv6055105, essv6158848, essv6119110, essv5965376, essv6218929, essv6483940, essv5901140, essv5887760, essv6310549, essv5554845, essv6278100, essv6244955, essv6002031, essv5538287, essv6009424, essv5712393, essv6561419, essv5942140, essv5912776, essv6263181, essv6582635, essv5732854, essv6398306, essv5922170, essv5521811, essv6587276, essv5465326, essv6242837, essv6364489, essv5431816, essv5769150, essv6298061, essv6424042, essv5760786, essv5843254, essv5655583, essv5690959, essv5665740, essv6349174, essv5520879, essv6270978, essv5774273, essv5704742, essv5731532, essv6142627, essv5679694, essv5723380, essv5824689, essv5421208, essv6538295, essv6198207, essv5642678, essv5446234, essv5708101, essv6450236, essv5402881, essv5856780, essv6186954, essv6400510, essv5418037, essv5465749, essv5512844, essv6542013, essv6034109
SamplesHG00096, HG01060, HG01441, HG00650, NA11830, HG01173, NA20543, NA19703, HG00536, HG00249, HG00671, HG01359, HG00257, HG01389, HG00699, NA20346, HG00654, NA18602, HG00693, NA18627, HG00271, NA07346, HG01250, NA19381, HG01366, HG01070, HG00251, HG01488, NA18635, NA18619, HG01492, NA19457, HG01069, HG01080, NA20278, HG00683, HG01170, HG00236, HG01072, NA19731, HG00422, HG00705, HG01440, HG00326, HG00323, HG01353, HG00543, HG00313, HG01136, HG00154, NA18613, HG01187, NA12003, HG01095, NA19455, NA19663, HG00436, HG00533, HG00275, NA18534, NA18548, HG01047, HG00324, HG00284, HG01073, HG00250, NA12829, NA18499, HG01101, HG00613, HG00525, NA19452, HG00463, NA18546, NA19834, NA18543, NA19749, NA19747, HG00353, HG00580, NA18941, HG01357, HG01375, HG01113, NA19083, NA18610, HG00125, NA20348, HG00259, NA18636, NA20289, HG00186, NA19770, HG00698, HG00280, HG00131, HG00274, NA18989, NA20322, NA12154, HG01437, HG01516
Known GenesPLCG2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665175
Frequency
Sample Size1151
Observed Gain0
Observed Loss102
Observed Complex0
Frequencyn/a


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