A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11614602



Internal ID6591882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134174996..134268650hg38UCSC Ensembl
chr4:135096151..135189805hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3893655
hg1993655
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602304
Supporting Variants
SamplesNA20768
Known GenesPABPC4L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11614602
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