A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660803



Internal ID9926908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125564814..126148324hg38UCSC Ensembl
chr4:126485969..127069479hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38583511
hg19583511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6421648, essv5501220, essv5600158, essv6041569, essv6538519
SamplesNA12842, NA20813, NA19062, NA20542, NA20804
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660803
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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