A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597353



Internal ID6984581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109492208..109500729hg38UCSC Ensembl
Innerchr3:109492243..109500694hg38UCSC Ensembl
Outerchr3:109492173..109500764hg38UCSC Ensembl
chr3:109211055..109219576hg19UCSC Ensembl
Innerchr3:109211090..109219541hg19UCSC Ensembl
Outerchr3:109211020..109219611hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg388522
hg198522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11098173, essv11098172
SamplesHG04042, HG03729
Known GenesFLJ25363
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597353
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