A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14214880



Internal ID696460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77572330..77575994hg38UCSC Ensembl
Innerchr11:77572330..77575994hg38UCSC Ensembl
Outerchr11:77572018..77576298hg38UCSC Ensembl
chr11:77283375..77287039hg19UCSC Ensembl
Innerchr11:77283375..77287039hg19UCSC Ensembl
Outerchr11:77283063..77287343hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg383665
hg193665
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626885
Supporting Variants
SamplesHG00327
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14214880
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