A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598389



Internal ID6638654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160767086..160857900hg38UCSC Ensembl
chr3:160484874..160575688hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg3890815
hg1990815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199782
SamplesHG03808
Known GenesPPM1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598389
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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