A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11370930



Internal ID5256545
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599959
Supporting Variants
SamplesNA18636
Known GenesPI4K2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11370930
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer