A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11572874



Internal ID1574690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:114600577..114660419hg38UCSC Ensembl
chr4:115521733..115581575hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3859843
hg1959843
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601835
Supporting Variants
SamplesHG03672
Known GenesMIR577, UGT8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11572874
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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