A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11021418



Internal ID4105830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58165586..58166607hg38UCSC Ensembl
Innerchr3:58165636..58166557hg38UCSC Ensembl
Outerchr3:58165536..58166657hg38UCSC Ensembl
chr3:58151313..58152334hg19UCSC Ensembl
Innerchr3:58151363..58152284hg19UCSC Ensembl
Outerchr3:58151263..58152384hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596241
Supporting Variants
SamplesHG03729
Known GenesFLNB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11021418
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