A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599824



Internal ID6986869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19821436..19823312hg38UCSC Ensembl
Innerchr4:19821436..19823312hg38UCSC Ensembl
Outerchr4:19821247..19823517hg38UCSC Ensembl
chr4:19823059..19824935hg19UCSC Ensembl
Innerchr4:19823059..19824935hg19UCSC Ensembl
Outerchr4:19822870..19825140hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381877
hg191877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11365921, essv11365919, essv11365916, essv11365901, essv11365915, essv11365928, essv11365925, essv11365931, essv11365892, essv11365908, essv11365902, essv11365918, essv11365924, essv11365896, essv11365929, essv11365894, essv11365920, essv11365905, essv11365899, essv11365923, essv11365922, essv11365904, essv11365893, essv11365898, essv11365906, essv11365926, essv11365900, essv11365913, essv11365903, essv11365909, essv11365910, essv11365914, essv11365927, essv11365897, essv11365930, essv11365911, essv11365895, essv11365917, essv11365912, essv11365907
SamplesNA19466, NA19098, NA19920, HG03464, HG03086, NA19307, HG02756, HG03479, HG02489, NA20278, NA19917, NA19024, HG03394, HG02977, HG03054, HG02678, NA18915, HG02450, HG01880, HG03202, HG02445, HG03446, HG03571, NA19338, HG03354, NA19160, HG02455, HG02721, HG01915, HG02923, HG03127, HG02941, HG03066, HG03313, NA19093, HG03538, HG03303, HG03439, NA19429, HG03271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599824
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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