A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625294



Internal ID6665442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7523852..7629549hg38UCSC Ensembl
chr11:7545083..7650780hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38105698
hg19105698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14014361, essv14014362
SamplesNA11933, HG01853
Known GenesPPFIBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625294
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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