A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625415



Internal ID7012249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13861685..13866465hg38UCSC Ensembl
Innerchr11:13862185..13865965hg38UCSC Ensembl
Outerchr11:13860685..13867465hg38UCSC Ensembl
chr11:13883232..13888012hg19UCSC Ensembl
Innerchr11:13883732..13887512hg19UCSC Ensembl
Outerchr11:13882232..13889012hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384781
hg194781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14033423
SamplesHG01857
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625415
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