A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11169098



Internal ID3589186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145092829..145177787hg38UCSC Ensembl
chr3:144810610..144895574hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3884959
hg1984965
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598056
Supporting Variants
SamplesHG03172
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11169098
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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