A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589816



Internal ID6977146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11346762..11357861hg38UCSC Ensembl
chr2:11486888..11497987hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3811100
hg1911100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10410386, essv10410389, essv10410387, essv10410388
SamplesNA19649, NA19651, NA19719, HG01174
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589816
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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