A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665701



Internal ID9931806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73452055..73465339hg38UCSC Ensembl
chr9:76066971..76080255hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3813285
hg1913285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6180180, essv6080141, essv5713014, essv6354815
SamplesNA18510, NA19374, NA19375, NA19116
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665701
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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