A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596980



Internal ID6984294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89895723..90040227hg38UCSC Ensembl
chr3:89944873..90089377hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38144505
hg19144505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11069212, essv11069211
SamplesHG03926, HG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596980
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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