A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6427837



Internal ID9753981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103981010..103985729hg38UCSC Ensembl
chr11:103851738..103856457hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384720
hg194720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671461
Supporting Variants
SamplesNA19704
Known GenesPDGFD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6427837
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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