A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891536



Internal ID19185932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5324922..5392243hg38UCSC Ensembl
Outerchr9:5324922..5392243hg38UCSC Ensembl
Innerchr9:5324922..5392243hg19UCSC Ensembl
Outerchr9:5324922..5392243hg19UCSC Ensembl
Innerchr9:5314922..5382243hg18UCSC Ensembl
Outerchr9:5314922..5382243hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3867322
hg1967322
hg1867322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783021, essv25796922, essv25798098, essv25786199, essv25785024, essv25786616, essv25796722
Samples
Known GenesPLGRKT, RLN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891536
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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