A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620671



Internal ID7007541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73445676..73447956hg38UCSC Ensembl
Innerchr9:73445681..73447951hg38UCSC Ensembl
Outerchr9:73445671..73447961hg38UCSC Ensembl
chr9:76060592..76062872hg19UCSC Ensembl
Innerchr9:76060597..76062867hg19UCSC Ensembl
Outerchr9:76060587..76062877hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13518800, essv13518805, essv13518806, essv13518798, essv13518811, essv13518804, essv13518797, essv13518809, essv13518815, essv13518799, essv13518814, essv13518801, essv13518813, essv13518812, essv13518803, essv13518808, essv13518802, essv13518810, essv13518807
SamplesHG02318, HG03515, HG03133, HG02620, HG03342, HG01069, NA19445, HG03120, NA18915, HG02976, HG01948, NA18858, HG03367, HG01939, NA19328, NA19129, HG03072, NA18522, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620671
Frequency
Sample Size2504
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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