A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891646



Internal ID19186042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26248037..26514108hg38UCSC Ensembl
Outerchr9:26248037..26514108hg38UCSC Ensembl
Innerchr9:26248035..26514106hg19UCSC Ensembl
Outerchr9:26248035..26514106hg19UCSC Ensembl
Innerchr9:26238035..26504106hg18UCSC Ensembl
Outerchr9:26238035..26504106hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38266072
hg19266072
hg18266072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783935
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891646
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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