A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11557574



Internal ID4636301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106710846..106721725hg38UCSC Ensembl
Innerchr4:106710846..106721725hg38UCSC Ensembl
Outerchr4:106710346..106722225hg38UCSC Ensembl
chr4:107632003..107642882hg19UCSC Ensembl
Innerchr4:107632003..107642882hg19UCSC Ensembl
Outerchr4:107631503..107643382hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3810880
hg1910880
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601693
Supporting Variants
SamplesHG04164
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11557574
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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