A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14111582



Internal ID1303993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42875552..42882513hg38UCSC Ensembl
chr11:42897102..42904063hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386962
hg196962
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626129
Supporting Variants
SamplesHG01140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14111582
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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