A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598285



Internal ID6985421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155760377..155780857hg38UCSC Ensembl
chr3:155478166..155498646hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3820481
hg1920481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191909, essv11191902, essv11191898, essv11191900, essv11191911, essv11191914, essv11191908, essv11191897, essv11191910, essv11191904, essv11191912, essv11191896, essv11191903, essv11191907, essv11191905, essv11191901, essv11191906, essv11191899, essv11191913
SamplesHG01326, HG01694, NA12813, NA20814, HG03016, NA20774, HG01710, HG00262, NA20811, HG00323, NA20506, HG01094, HG01161, HG01679, NA12043, HG00254, HG00734, HG00131, NA19780
Known GenesC3orf33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598285
Frequency
Sample Size2504
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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