A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598056



Internal ID6985192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145092829..145177787hg38UCSC Ensembl
chr3:144810610..144895574hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3884959
hg1984965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv944e214
Supporting Variantsessv11169098, essv11169097, essv11169099
SamplesHG03172, HG02317, NA19818
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598056
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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