A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11543897



Internal ID4716562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100767021..100772145hg38UCSC Ensembl
Innerchr4:100767021..100772145hg38UCSC Ensembl
Outerchr4:100766803..100772314hg38UCSC Ensembl
chr4:101688178..101693302hg19UCSC Ensembl
Innerchr4:101688178..101693302hg19UCSC Ensembl
Outerchr4:101687960..101693471hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg385125
hg195125
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601582
Supporting Variants
SamplesHG04238
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11543897
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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