A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596975



Internal ID6984289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89801126..90128234hg38UCSC Ensembl
chr3:89850276..90177384hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38327109
hg19327109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069201, essv11069200
SamplesHG03926, HG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596975
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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