A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890737



Internal ID19185039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166577538..166613055hg38UCSC Ensembl
Outerchr1:166566961..166642976hg38UCSC Ensembl
Innerchr1:166546775..166582292hg19UCSC Ensembl
Outerchr1:166536198..166612213hg19UCSC Ensembl
Innerchr1:164813399..164848916hg18UCSC Ensembl
Outerchr1:164802822..164878837hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3876016
hg1976016
hg1876016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787182, essv25780576, essv25780951, essv25780896, essv25785290, essv25798977
Samples
Known GenesFMO9P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890737
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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