A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891730



Internal ID19186126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129342864..129353781hg38UCSC Ensembl
Outerchr9:129342864..129353781hg38UCSC Ensembl
Innerchr9:132105143..132116060hg19UCSC Ensembl
Outerchr9:132105143..132116060hg19UCSC Ensembl
Innerchr9:131144964..131155881hg18UCSC Ensembl
Outerchr9:131144964..131155881hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3810918
hg1910918
hg1810918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778804
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891730
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