A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668279



Internal ID9587698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46399316..46401005hg38UCSC Ensembl
chr10:47148758..47150447hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5544134, essv5761641, essv5478872, essv6428321, essv6464147, essv5908076, essv5834880, essv6578235, essv5481942, essv6110599, essv6591135, essv5680964, essv6289230, essv6354340, essv6418447, essv6136001, essv5636449, essv6183386
SamplesNA19712, NA19819, HG00131, NA19435, NA19338, NA19461, NA19701, NA19355, NA18912, NA19440, HG01136, NA19313, NA19711, NA19376, NA18909, NA19381, NA19385, NA18519
Known GenesLINC00842
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668279
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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