A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601693



Internal ID6988729
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11557574
SamplesHG04164
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601693
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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