A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11158466



Internal ID1160282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136980610..137047680hg38UCSC Ensembl
chr3:136699452..136766522hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3867071
hg1967071
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597894
Supporting Variants
SamplesHG03890
Known GenesIL20RB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11158466
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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