A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11176503



Internal ID470996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147766890..147888706hg38UCSC Ensembl
chr3:147484677..147606493hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38121817
hg19121817
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598118
Supporting Variants
SamplesHG00151
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11176503
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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