A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11098172



Internal ID4105772
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597353
Supporting Variants
SamplesHG03729
Known GenesFLJ25363
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11098172
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