A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799669



Internal ID19170510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115855252..115903186hg38UCSC Ensembl
Innerchr9:118617531..118665465hg19UCSC Ensembl
Innerchr9:117657352..117705286hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3847935
hg1947935
hg1847935
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891718
Supporting Variants
Samples
Known GenesLINC00474
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799669
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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