A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11366035



Internal ID3163360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20206330..20209454hg38UCSC Ensembl
Innerchr4:20206330..20209454hg38UCSC Ensembl
Outerchr4:20206116..20209651hg38UCSC Ensembl
chr4:20207953..20211077hg19UCSC Ensembl
Innerchr4:20207953..20211077hg19UCSC Ensembl
Outerchr4:20207739..20211274hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383125
hg193125
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599839
Supporting Variants
SamplesHG02784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11366035
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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