A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586381



Internal ID6973902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71319075..71388961hg38UCSC Ensembl
chr1:71784758..71854644hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3869887
hg1969887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9964934
SamplesHG00139
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586381
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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