A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658453



Internal ID9924558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103694209..103694403hg38UCSC Ensembl
chr4:104615366..104615560hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6157415, essv6529202, essv5669041, essv5554961, essv6278204, essv5841533, essv5727324, essv6364978, essv6452590, essv6380111, essv6252294, essv5526859, essv5797481, essv6114060, essv5591180, essv6262470, essv5512088, essv5639425, essv5518811, essv6356119, essv6044970, essv6200288, essv5951579
SamplesNA19703, NA18947, NA18508, NA18980, NA18486, NA19098, NA18526, NA18489, NA18923, NA18960, NA18916, NA11918, NA18498, NA19172, NA19239, NA18956, NA18566, NA18912, NA18576, NA18961, NA18517, NA20276, NA12006
Known GenesTACR3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658453
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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