A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11390797



Internal ID5668840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33668101..33679138hg38UCSC Ensembl
Innerchr4:33668147..33679092hg38UCSC Ensembl
Outerchr4:33668055..33679184hg38UCSC Ensembl
chr4:33669723..33680760hg19UCSC Ensembl
Innerchr4:33669769..33680714hg19UCSC Ensembl
Outerchr4:33669677..33680806hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3811038
hg1911038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600157
Supporting Variants
SamplesNA19076
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11390797
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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