A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11557435



Internal ID4666695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106525524..106545735hg38UCSC Ensembl
Innerchr4:106525526..106545734hg38UCSC Ensembl
Outerchr4:106525523..106545737hg38UCSC Ensembl
chr4:107446681..107466892hg19UCSC Ensembl
Innerchr4:107446683..107466891hg19UCSC Ensembl
Outerchr4:107446680..107466894hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3820212
hg1920212
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601691
Supporting Variants
SamplesHG04194
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11557435
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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