A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891093



Internal ID19185489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:208472745..208944955hg38UCSC Ensembl
Outerchr1:208472745..208944955hg38UCSC Ensembl
Innerchr1:208646090..209118300hg19UCSC Ensembl
Outerchr1:208646090..209118300hg19UCSC Ensembl
Innerchr1:206712713..207184923hg18UCSC Ensembl
Outerchr1:206712713..207184923hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38472211
hg19472211
hg18472211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792404
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891093
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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