A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893740



Internal ID19184560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90297978..90390153hg38UCSC Ensembl
Outerchr3:90289369..90444732hg38UCSC Ensembl
Innerchr3:90347128..90439303hg19UCSC Ensembl
Outerchr3:90338519..90493882hg19UCSC Ensembl
Innerchr3:90429818..90521993hg18UCSC Ensembl
Outerchr3:90421209..90576572hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38155364
hg19155364
hg18155364
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787121, essv25800758, essv25799830, essv25799811, essv25787362, essv25792727, essv25787088, essv25789744
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893740
Frequency
Sample Size3017
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


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