A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663713



Internal ID9929818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86842993..86843358hg38UCSC Ensembl
chr9:89457908..89458273hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5428650, essv6216216, essv6516181, essv5985308, essv5700974, essv5678442, essv6183633, essv6098307, essv5608317, essv6151564, essv6296699, essv5894336, essv6123866, essv5823952, essv5431405, essv5531747, essv6117502, essv5432904, essv6050243, essv5930745, essv5611279, essv5960259, essv6340562, essv5688481, essv5754365, essv6393206, essv5744407, essv5897865, essv6538025, essv6064088, essv6512629, essv6517720, essv5831709
SamplesNA18502, NA19701, NA19704, NA18486, NA19190, NA20356, NA07346, NA19379, NA19723, NA19131, NA18960, NA19372, NA19317, NA19159, NA19189, NA18520, NA18934, NA19455, NA18912, NA19338, NA18523, NA18858, NA19440, NA18961, NA19712, NA19434, NA19428, NA19311, NA19360, NA19093, NA18989, NA18511, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663713
Frequency
Sample Size1151
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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