A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11377162



Internal ID6692866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:28348428..28359213hg38UCSC Ensembl
Innerchr4:28348452..28359189hg38UCSC Ensembl
Outerchr4:28348404..28359237hg38UCSC Ensembl
chr4:28350050..28360835hg19UCSC Ensembl
Innerchr4:28350074..28360811hg19UCSC Ensembl
Outerchr4:28350026..28360859hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3810786
hg1910786
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600019
Supporting Variants
SamplesNA20821
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11377162
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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