A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892303



Internal ID18836437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16886874..16941001hg38UCSC Ensembl
Outerchr1:16856620..16955930hg38UCSC Ensembl
Innerchr1:17213369..17267496hg19UCSC Ensembl
Outerchr1:17183115..17282425hg19UCSC Ensembl
Innerchr1:17085956..17140083hg18UCSC Ensembl
Outerchr1:17055702..17155012hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3899311
hg1999311
hg1899311
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786037, essv25784995, essv25798913, essv25786129, essv25800967, essv25791145, essv25785742
Samples
Known GenesCROCC, MIR3675
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892303
Frequency
Sample Size3017
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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