A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627277



Internal ID7014107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92498634..92511135hg38UCSC Ensembl
Innerchr11:92498634..92511135hg38UCSC Ensembl
Outerchr11:92498464..92511205hg38UCSC Ensembl
chr11:92231800..92244301hg19UCSC Ensembl
Innerchr11:92231800..92244301hg19UCSC Ensembl
Outerchr11:92231630..92244371hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812502
hg1912502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14234152
SamplesHG02477
Known GenesFAT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627277
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