A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891645



Internal ID19186041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26248037..26276394hg38UCSC Ensembl
Outerchr9:26248037..26276394hg38UCSC Ensembl
Innerchr9:26248035..26276392hg19UCSC Ensembl
Outerchr9:26248035..26276392hg19UCSC Ensembl
Innerchr9:26238035..26266392hg18UCSC Ensembl
Outerchr9:26238035..26266392hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3828358
hg1928358
hg1828358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780195
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891645
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