A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659877



Internal ID9925982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72069561..72074830hg38UCSC Ensembl
chr9:74684477..74689746hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385270
hg195270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6463338, essv6475127, essv5738351, essv6250839, essv5655490, essv5928487
SamplesNA12842, NA12340, NA12718, HG01047, HG01197, HG01108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659877
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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