A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628068



Internal ID7014893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129624413..129625979hg38UCSC Ensembl
Innerchr11:129624430..129625963hg38UCSC Ensembl
Outerchr11:129624397..129625996hg38UCSC Ensembl
chr11:129494308..129495874hg19UCSC Ensembl
Innerchr11:129494325..129495858hg19UCSC Ensembl
Outerchr11:129494292..129495891hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381567
hg191567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14310166, essv14310167
SamplesHG03808, HG02649
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628068
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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