A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599333



Internal ID6986381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198025659..198052867hg38UCSC Ensembl
chr3:197752530..197779738hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3827209
hg1927209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11312944, essv11312946, essv11312945, essv11312942, essv11312943
SamplesHG00179, HG03604, NA19184, NA19031, HG00410
Known GenesLMLN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599333
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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