A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893651



Internal ID19184471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6446415..6524190hg38UCSC Ensembl
Outerchr3:6440687..6524190hg38UCSC Ensembl
Innerchr3:6488102..6565877hg19UCSC Ensembl
Outerchr3:6482374..6565877hg19UCSC Ensembl
Innerchr3:6463102..6540877hg18UCSC Ensembl
Outerchr3:6457374..6540877hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3883504
hg1983504
hg1883504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797980, essv25799156, essv25800994, essv25784348, essv25797988, essv25780833
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893651
Frequency
Sample Size3017
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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