A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891798



Internal ID19186194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45052581..45208304hg38UCSC Ensembl
Outerchr10:45052581..45208304hg38UCSC Ensembl
Innerchr10:45548029..45703752hg19UCSC Ensembl
Outerchr10:45548029..45703752hg19UCSC Ensembl
Innerchr10:44868035..45023758hg18UCSC Ensembl
Outerchr10:44868035..45023758hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38155724
hg19155724
hg18155724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787967
Samples
Known GenesANKRD30BP3, MIR3156-1, RSU1P2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891798
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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