A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892816



Internal ID19183636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22626894..22766456hg38UCSC Ensembl
Outerchr16:22620078..22766456hg38UCSC Ensembl
Innerchr16:22638215..22777777hg19UCSC Ensembl
Outerchr16:22631399..22777777hg19UCSC Ensembl
Innerchr16:22545716..22685278hg18UCSC Ensembl
Outerchr16:22538900..22685278hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38146379
hg19146379
hg18146379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788195, essv25792871
Samples
Known GenesMIR548AA2, MIR548D2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892816
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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