A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891655



Internal ID19186051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31215244..31255728hg38UCSC Ensembl
Outerchr9:31209671..31264081hg38UCSC Ensembl
Innerchr9:31215242..31255726hg19UCSC Ensembl
Outerchr9:31209669..31264079hg19UCSC Ensembl
Innerchr9:31205242..31245726hg18UCSC Ensembl
Outerchr9:31199669..31254079hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3854411
hg1954411
hg1854411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782421, essv25797545, essv25796888
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891655
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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