A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625788



Internal ID7012622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28999052..29007052hg38UCSC Ensembl
Innerchr11:28999552..29006552hg38UCSC Ensembl
Outerchr11:28998052..29008052hg38UCSC Ensembl
chr11:29020599..29028599hg19UCSC Ensembl
Innerchr11:29021099..29028099hg19UCSC Ensembl
Outerchr11:29019599..29029599hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14075296, essv14075298, essv14075297
SamplesHG03556, HG02309, HG01886
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625788
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer