A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13993488



Internal ID5240371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1648252..1662145hg38UCSC Ensembl
chr11:1669482..1683375hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813894
hg1913894
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625114
Supporting Variants
SamplesNA18630
Known GenesMOB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13993488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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