A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891605



Internal ID19186001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11967114..12405940hg38UCSC Ensembl
Outerchr9:11967114..12405940hg38UCSC Ensembl
Innerchr9:11967114..12405940hg19UCSC Ensembl
Outerchr9:11967114..12405940hg19UCSC Ensembl
Innerchr9:11957114..12395940hg18UCSC Ensembl
Outerchr9:11957114..12395940hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38438827
hg19438827
hg18438827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778379
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891605
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer