A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665296



Internal ID9931401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14686712..14688580hg38UCSC Ensembl
Outerchr9:14686675..14688630hg38UCSC Ensembl
Innerchr9:14686710..14688578hg19UCSC Ensembl
Outerchr9:14686673..14688628hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381956
hg191956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1326e199
Supporting Variantsessv5903992, essv5818652, essv5599101, essv5656568, essv5458897, essv5769112, essv5953784, essv5516482, essv5629527, essv6255287, essv5895756, essv6201449, essv6162215, essv5568762, essv5635701
SamplesNA19703, NA18508, NA18916, NA18498, NA18868, NA19238, NA18871, NA18907, NA18499, NA18858, NA19108, NA19147, NA19818, NA19093, NA18522
Known GenesZDHHC21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665296
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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