A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891530



Internal ID19185926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4400991..4483912hg38UCSC Ensembl
Outerchr9:4400991..4483912hg38UCSC Ensembl
Innerchr9:4400991..4483912hg19UCSC Ensembl
Outerchr9:4400991..4483912hg19UCSC Ensembl
Innerchr9:4390991..4473912hg18UCSC Ensembl
Outerchr9:4390991..4473912hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3882922
hg1982922
hg1882922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781140
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891530
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