A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6351486



Internal ID9328889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47740285..47741686hg38UCSC Ensembl
chr11:47761837..47763238hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676370
Supporting Variants
SamplesNA19819
Known GenesFNBP4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6351486
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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