A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660518



Internal ID9926623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47227890..47228139hg38UCSC Ensembl
chr15:47520087..47520336hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6349050, essv6245916, essv6173717, essv5992413, essv5685097, essv5449922, essv6070590, essv5984893, essv6404790, essv6173991, essv6411120, essv5855028, essv5752960, essv6453336, essv6020046, essv5682144, essv6582769, essv5606027, essv5993711, essv6358672, essv6185533
SamplesNA18959, NA18563, HG00501, HG00512, HG00534, HG00557, HG00653, HG00436, NA18579, NA18572, NA18534, HG00684, NA18536, HG00580, HG00418, HG00672, HG00614, HG00421, HG00698, NA18623, NA18612
Known GenesSEMA6D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660518
Frequency
Sample Size1151
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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