A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890859



Internal ID19185161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10281458..10325606hg38UCSC Ensembl
Outerchr1:10281458..10325606hg38UCSC Ensembl
Innerchr1:10341516..10385664hg19UCSC Ensembl
Outerchr1:10341516..10385664hg19UCSC Ensembl
Innerchr1:10264103..10308251hg18UCSC Ensembl
Outerchr1:10264103..10308251hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3844149
hg1944149
hg1844149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784884
Samples
Known GenesKIF1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890859
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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