A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14058108



Internal ID3120796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23934910..23942366hg38UCSC Ensembl
Innerchr11:23935060..23942216hg38UCSC Ensembl
Outerchr11:23934760..23942516hg38UCSC Ensembl
chr11:23956456..23963912hg19UCSC Ensembl
Innerchr11:23956606..23963762hg19UCSC Ensembl
Outerchr11:23956306..23964062hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg387457
hg197457
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625658
Supporting Variants
SamplesHG02737
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14058108
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