A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11357081



Internal ID4574751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11624709..11858769hg38UCSC Ensembl
Innerchr4:11624709..11858769hg38UCSC Ensembl
Outerchr4:11624209..11859269hg38UCSC Ensembl
chr4:11626333..11860393hg19UCSC Ensembl
Innerchr4:11626333..11860393hg19UCSC Ensembl
Outerchr4:11625833..11860893hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38234061
hg19234061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599652
Supporting Variants
SamplesHG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11357081
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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