A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594882



Internal ID6982201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123413..148333hg38UCSC Ensembl
chr3:165096..190016hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3824921
hg1924921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10896256, essv10896258, essv10896257
SamplesHG01880, HG02725, HG02238
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594882
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