A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599331



Internal ID6639596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197953544..197984148hg38UCSC Ensembl
chr3:197680415..197711019hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3830605
hg1930605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11312935, essv11312934, essv11312933, essv11312936
SamplesNA19031, NA19184, HG03604, HG00410
Known GenesIQCG, LMLN, RPL35A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599331
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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