A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894180



Internal ID19185249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41229175..41241508hg38UCSC Ensembl
Outerchr5:41229175..41241508hg38UCSC Ensembl
Innerchr5:41229277..41241610hg19UCSC Ensembl
Outerchr5:41229277..41241610hg19UCSC Ensembl
Innerchr5:41265034..41277367hg18UCSC Ensembl
Outerchr5:41265034..41277367hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3812334
hg1912334
hg1812334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785819, essv25779612, essv25784013, essv25801360, essv25785344
Samples
Known GenesC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894180
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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