A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891534



Internal ID19185930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4903818..4911930hg38UCSC Ensembl
Outerchr9:4895947..4911930hg38UCSC Ensembl
Innerchr9:4903818..4911930hg19UCSC Ensembl
Outerchr9:4895947..4911930hg19UCSC Ensembl
Innerchr9:4893818..4901930hg18UCSC Ensembl
Outerchr9:4885947..4901930hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3815984
hg1915984
hg1815984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782628, essv25800247
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891534
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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