A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586209



Internal ID6973729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60535296..60607501hg38UCSC Ensembl
chr1:61000968..61073173hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3872206
hg1972206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9945936, essv9945937
SamplesNA21111, NA21089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586209
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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