A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14043963



Internal ID2228857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18920189..18942450hg38UCSC Ensembl
chr11:18941736..18963997hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822262
hg1922262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625519
Supporting Variants
SamplesHG02003
Known GenesMRGPRX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14043963
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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