A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625293



Internal ID6665441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7515685..7685956hg38UCSC Ensembl
chr11:7536916..7707187hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38170272
hg19170272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14014359, essv14014360
SamplesNA11933, HG01853
Known GenesCYB5R2, PPFIBP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625293
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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