A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623741



Internal ID7010597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69297614..69300767hg38UCSC Ensembl
Innerchr10:69297620..69300762hg38UCSC Ensembl
Outerchr10:69297609..69300773hg38UCSC Ensembl
chr10:71057370..71060523hg19UCSC Ensembl
Innerchr10:71057376..71060518hg19UCSC Ensembl
Outerchr10:71057365..71060529hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383154
hg193154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13855059, essv13855051, essv13855018, essv13855039, essv13855060, essv13855078, essv13855055, essv13855070, essv13855052, essv13855046, essv13855038, essv13855025, essv13855058, essv13855035, essv13855017, essv13855076, essv13855072, essv13855006, essv13855045, essv13855063, essv13855016, essv13855020, essv13855013, essv13855048, essv13855023, essv13855034, essv13855024, essv13855029, essv13855026, essv13855007, essv13855008, essv13855067, essv13855065, essv13855053, essv13855005, essv13855030, essv13855068, essv13855003, essv13855041, essv13855069, essv13855066, essv13855014, essv13855050, essv13855009, essv13855073, essv13855031, essv13855054, essv13855077, essv13855071, essv13855042, essv13855032, essv13855062, essv13855075, essv13855022, essv13855027, essv13855074, essv13855004, essv13855036, essv13855015, essv13855056, essv13855064, essv13855040, essv13855011, essv13855043, essv13855019, essv13855033, essv13855037, essv13855010, essv13855044, essv13855057, essv13855021, essv13855028, essv13855061, essv13855047, essv13855012, essv13855049
SamplesHG02890, HG02628, HG03052, NA19204, HG01885, HG01079, HG03300, HG03449, NA18917, HG03558, HG02870, HG03521, HG03298, HG02624, HG03295, HG03126, HG03193, NA18870, HG03069, HG02895, HG03572, HG03436, HG03135, HG02840, NA19198, HG02756, HG03105, NA20287, NA19130, NA19041, NA18874, HG03268, HG02634, NA19159, HG03058, HG02623, NA19445, HG03583, HG02715, NA19200, HG02977, HG03132, NA19236, HG02322, HG01880, HG03202, HG02884, HG02309, HG02881, HG02283, HG03451, HG02979, HG01890, HG03567, HG02772, NA20296, HG03064, HG03461, HG03437, HG01551, NA19331, HG02837, HG02317, NA19360, HG02814, HG02771, NA19376, NA19143, HG02646, HG02938, NA20289, NA19096, HG03470, HG03445, HG01111, HG02629
Known GenesHK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623741
Frequency
Sample Size2504
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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