A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891550



Internal ID19185946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7668843..7735283hg38UCSC Ensembl
Outerchr9:7668843..7735283hg38UCSC Ensembl
Innerchr9:7668843..7735283hg19UCSC Ensembl
Outerchr9:7668843..7735283hg19UCSC Ensembl
Innerchr9:7658843..7725283hg18UCSC Ensembl
Outerchr9:7658843..7725283hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3866441
hg1966441
hg1866441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783521
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891550
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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