A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3591126



Internal ID6978454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66638640..66649195hg38UCSC Ensembl
chr2:66865772..66876327hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3810556
hg1910556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10532384, essv10532383
SamplesHG03224, HG02594
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3591126
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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