A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14234152



Internal ID2805326
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627277
Supporting Variants
SamplesHG02477
Known GenesFAT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14234152
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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