A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11272666



Internal ID785357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191634598..191712717hg38UCSC Ensembl
chr3:191352387..191430506hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3878120
hg1978120
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599118
Supporting Variants
SamplesHG00371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11272666
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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