A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643803



Internal ID7030560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16703946..16705755hg38UCSC Ensembl
Innerchr19:16704446..16705255hg38UCSC Ensembl
Outerchr19:16702946..16706755hg38UCSC Ensembl
chr19:16814757..16816566hg19UCSC Ensembl
Innerchr19:16815257..16816066hg19UCSC Ensembl
Outerchr19:16813757..16817566hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381810
hg191810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002864, essv16002835, essv16002865, essv16002860, essv16002841, essv16002842, essv16002859, essv16002834, essv16002852, essv16002846, essv16002840, essv16002854, essv16002856, essv16002826, essv16002855, essv16002838, essv16002858, essv16002863, essv16002829, essv16002861, essv16002845, essv16002848, essv16002844, essv16002830, essv16002850, essv16002862, essv16002839, essv16002833, essv16002853, essv16002849, essv16002851, essv16002831, essv16002857, essv16002832, essv16002843, essv16002827, essv16002847, essv16002836, essv16002837, essv16002828
SamplesHG03449, HG02836, HG02476, HG03139, HG02536, HG02895, HG03478, NA18923, HG02840, HG03209, HG03556, NA19917, HG03212, NA19235, NA19385, HG02571, HG02623, NA20318, HG03048, NA19247, HG03061, NA18915, HG02878, HG03472, NA19113, HG02568, HG02772, HG02813, HG02799, HG01958, HG02923, HG02317, HG02814, NA19475, NA19376, HG03066, HG03401, HG02465, HG02808, HG02629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643803
Frequency
Sample Size2504
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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