A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619870



Internal ID7006744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18298060..18320068hg38UCSC Ensembl
chr9:18298058..18320066hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3822009
hg1922009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415092, essv13415085, essv13415093, essv13415086, essv13415079, essv13415083, essv13415094, essv13415078, essv13415082, essv13415087, essv13415080, essv13415081, essv13415077, essv13415090, essv13415089, essv13415088, essv13415075, essv13415076, essv13415091, essv13415084
SamplesHG03690, HG03800, NA21089, NA21100, NA21115, NA21137, NA21128, NA20861, HG03746, NA20884, HG02793, HG04026, HG02696, HG03899, NA21125, HG03733, NA20852, NA21093, HG03872, NA21091
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619870
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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