A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602304



Internal ID6989338
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11614602, essv11614601
SamplesNA20768, HG01357
Known GenesPABPC4L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602304
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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