A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599959



Internal ID6987003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25219862..25235691hg38UCSC Ensembl
chr4:25221484..25237313hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3815830
hg1915830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370930
SamplesNA18636
Known GenesPI4K2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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