A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3447097



Internal ID15294047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3570827..3611625hg38UCSC Ensembl
Innerchr4:3571827..3610625hg38UCSC Ensembl
Outerchr4:3569827..3612625hg38UCSC Ensembl
chr4:3572554..3613352hg19UCSC Ensembl
Innerchr4:3573554..3612352hg19UCSC Ensembl
Outerchr4:3571554..3614352hg19UCSC Ensembl
chr4:3542352..3583150hg18UCSC Ensembl
Innerchr4:3543352..3582150hg18UCSC Ensembl
Outerchr4:3541352..3584150hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3840799
hg1940799
hg1840799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8694394
SamplesNA19240
Known GenesLINC00955
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3447097
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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