A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11552245



Internal ID4011754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104675866..104688684hg38UCSC Ensembl
Innerchr4:104675931..104688620hg38UCSC Ensembl
Outerchr4:104675802..104688749hg38UCSC Ensembl
chr4:105597023..105609841hg19UCSC Ensembl
Innerchr4:105597088..105609777hg19UCSC Ensembl
Outerchr4:105596959..105609906hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3812819
hg1912819
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601651
Supporting Variants
SamplesHG03667
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11552245
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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