A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598932



Internal ID6639197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183868888..183872993hg38UCSC Ensembl
Innerchr3:183868906..183872975hg38UCSC Ensembl
Outerchr3:183868870..183873011hg38UCSC Ensembl
chr3:183586676..183590781hg19UCSC Ensembl
Innerchr3:183586694..183590763hg19UCSC Ensembl
Outerchr3:183586658..183590799hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg384106
hg194106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11253152
SamplesHG03209
Known GenesPARL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598932
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