A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789479



Internal ID19179200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:43614545..43675867hg19UCSC Ensembl
Innerchr9:43554541..43615863hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg1961323
hg1861323
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891672
Supporting Variants
Samples
Known GenesSPATA31A6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789479
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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