A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586157



Internal ID6973677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58256360..58270320hg38UCSC Ensembl
chr1:58722032..58735992hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3813961
hg1913961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9938821, essv9938823, essv9938818, essv9938814, essv9938815, essv9938822, essv9938819, essv9938816, essv9938820, essv9938817
SamplesHG02385, HG01806, NA20756, HG00137, HG02057, HG01936, HG01257, HG00125, HG02348, HG02028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586157
Frequency
Sample Size2504
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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