A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11373444



Internal ID4118942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26030610..26038435hg38UCSC Ensembl
Innerchr4:26030610..26038435hg38UCSC Ensembl
Outerchr4:26030473..26038598hg38UCSC Ensembl
chr4:26032232..26040057hg19UCSC Ensembl
Innerchr4:26032232..26040057hg19UCSC Ensembl
Outerchr4:26032095..26040220hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387826
hg197826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599978
Supporting Variants
SamplesHG03738
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11373444
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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