A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598349



Internal ID6985485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159018011..159054591hg38UCSC Ensembl
chr3:158735800..158772380hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3836581
hg1936581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11198358, essv11198357
SamplesHG02298, HG03919
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598349
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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