A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890748



Internal ID19185050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10093095..10170448hg38UCSC Ensembl
Outerchr1:10093095..10170448hg38UCSC Ensembl
Innerchr1:10153153..10230506hg19UCSC Ensembl
Outerchr1:10153153..10230506hg19UCSC Ensembl
Innerchr1:10075740..10153093hg18UCSC Ensembl
Outerchr1:10075740..10153093hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3877354
hg1977354
hg1877354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787927
Samples
Known GenesUBE4B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890748
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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