A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670936



Internal ID9937041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107564090..107564924hg38UCSC Ensembl
chr9:110326371..110327205hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6335939, essv6431430, essv6595743, essv6467828, essv6057902, essv5928783, essv5909762, essv6509823, essv5434648, essv5697637, essv5653515
SamplesNA19107, NA18489, NA07347, NA19383, NA19239, NA18909, NA19108, NA19256, NA18517, NA19472, NA18522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670936
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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