A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658212



Internal ID9924317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63270287..63271637hg38UCSC Ensembl
Outerchr10:63270231..63271699hg38UCSC Ensembl
Innerchr10:65030047..65031397hg19UCSC Ensembl
Outerchr10:65029991..65031459hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381469
hg191469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6144053, essv6216741, essv6374885, essv6054731, essv6527936, essv6159652, essv6348243, essv5860527, essv5407257, essv6526386, essv6591170, essv5725681, essv5864688, essv5943031
SamplesNA11920, NA12889, NA19921, NA18566, NA12829, NA18499, NA12778, NA19401, NA12716, NA20778, NA19711, NA18552, NA18624, NA19429
Known GenesJMJD1C
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658212
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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