A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597196



Internal ID6984510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101802374..101802932hg38UCSC Ensembl
Innerchr3:101802377..101802929hg38UCSC Ensembl
Outerchr3:101802371..101802935hg38UCSC Ensembl
chr3:101521218..101521776hg19UCSC Ensembl
Innerchr3:101521221..101521773hg19UCSC Ensembl
Outerchr3:101521215..101521779hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11088804, essv11088817, essv11088801, essv11088808, essv11088795, essv11088776, essv11088813, essv11088780, essv11088779, essv11088811, essv11088807, essv11088789, essv11088806, essv11088788, essv11088790, essv11088800, essv11088773, essv11088778, essv11088815, essv11088786, essv11088822, essv11088785, essv11088783, essv11088787, essv11088782, essv11088771, essv11088820, essv11088784, essv11088818, essv11088797, essv11088825, essv11088821, essv11088823, essv11088796, essv11088792, essv11088824, essv11088803, essv11088794, essv11088774, essv11088781, essv11088777, essv11088805, essv11088791, essv11088812, essv11088775, essv11088798, essv11088809, essv11088770, essv11088810, essv11088802, essv11088793, essv11088799, essv11088819, essv11088816, essv11088814, essv11088772
SamplesHG02890, HG03366, HG03484, HG02702, HG03517, HG03057, HG03241, HG02419, HG02891, HG03295, HG03139, HG02536, HG03372, HG03133, HG03135, NA18489, HG03485, NA19131, HG03578, HG02054, HG03079, NA18874, NA19207, HG02588, NA18520, HG02946, HG02623, HG03055, HG03048, HG02977, NA19327, NA19982, HG03575, NA18871, HG03472, HG03301, NA19114, HG01241, HG03567, HG02772, HG03240, HG03367, HG01915, NA19435, HG03469, HG03433, HG03127, HG02464, HG03108, HG02771, HG02938, NA19713, NA19096, HG03401, NA19146, HG02760
Known GenesNXPE3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597196
Frequency
Sample Size2504
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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