A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674215



Internal ID9940320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23290081..23299891hg38UCSC Ensembl
chr9:23290079..23299889hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389811
hg199811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6532897, essv5477580, essv5781267, essv6453095, essv6202591, essv6183702, essv5807979, essv5628537, essv5662086, essv6277106, essv6132137, essv6564219, essv5815214, essv6597574, essv6242397, essv6215751, essv6120131, essv5973210
SamplesNA18592, NA18599, NA19067, NA19076, NA19649, NA19782, NA19789, HG00577, NA19788, NA19658, NA19064, NA19655, NA18950, HG00638, NA19083, NA19726, NA19661, NA18612
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674215
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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