A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786199



Internal ID19165786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5324922..5392243hg38UCSC Ensembl
Innerchr9:5324922..5392243hg19UCSC Ensembl
Innerchr9:5314922..5382243hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3867322
hg1967322
hg1867322
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891536
Supporting Variants
Samples
Known GenesPLGRKT, RLN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786199
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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