A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663935



Internal ID9930040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32164918..32165056hg38UCSC Ensembl
chr10:32453846..32453984hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6295068, essv6169113, essv5600615, essv5601318, essv6490800, essv5931061, essv6071826, essv6398997, essv5491586, essv5597420, essv6369335, essv5636695, essv6560956, essv5739248, essv5633891, essv5758796, essv6162463, essv5461243, essv5410251, essv5597192, essv6582632, essv5588671, essv5905836, essv6231683, essv6386825, essv6524179, essv6081595, essv6423303, essv5468222, essv5510927, essv6376919, essv6305456, essv6446475, essv6052691, essv5474784, essv6196147, essv5738617, essv6322571, essv6190911, essv6038172, essv5546728, essv6171768
SamplesNA18561, HG00699, HG00261, HG00337, HG00138, HG00448, HG00330, HG00346, HG01365, NA20513, HG00325, HG00534, HG00309, NA18557, HG00253, HG00108, HG01171, HG00557, HG00701, HG00436, HG00533, HG00583, NA18566, HG00284, HG01073, HG00479, HG00331, HG01101, HG00613, NA18570, HG01107, NA18632, NA18543, HG01174, HG00256, NA06986, HG00614, HG00421, HG00343, NA18623, NA18612, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663935
Frequency
Sample Size1151
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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