A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586601



Internal ID6974119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:80708204..80798262hg38UCSC Ensembl
chr1:81173889..81263947hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3890059
hg1990059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9989330
SamplesHG03629
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586601
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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