A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3421978



Internal ID15268936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122804292..122804305hg38UCSC Ensembl
Innerchr10:122804282..122804313hg38UCSC Ensembl
Outerchr10:122804269..122804326hg38UCSC Ensembl
chr10:124563808..124563821hg19UCSC Ensembl
Innerchr10:124563798..124563829hg19UCSC Ensembl
Outerchr10:124563785..124563842hg19UCSC Ensembl
chr10:124553798..124553811hg18UCSC Ensembl
Innerchr10:124553819..124553788hg18UCSC Ensembl
Outerchr10:124553775..124553832hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8950892, essv8950899, essv8950873, essv8950866, essv8950871, essv8950900, essv8950876, essv8950883, essv8950894, essv8950887, essv8950884, essv8950881, essv8950888, essv8950882, essv8950870, essv8950875, essv8950877, essv8950880, essv8950863, essv8950898, essv8950896, essv8950865, essv8950897, essv8950893, essv8950869, essv8950872, essv8950885, essv8950874, essv8950878, essv8950889, essv8950867, essv8950886, essv8950864, essv8950895
SamplesNA18947, NA11995, NA18861, NA10851, NA18561, NA18944, NA18940, NA18558, NA11992, NA18582, NA18571, NA12044, NA18973, NA18638, NA10847, NA18605, NA12003, NA18516, NA18572, NA18948, NA18537, NA18566, NA18573, NA19114, NA18608, NA18542, NA18952, NA18564, NA18943, NA12763, NA18609, NA12006, NA18965, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3421978
Frequency
Sample Size185
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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