A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780331



Internal ID19180992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96360020..96393335hg38UCSC Ensembl
Innerchr3:96078864..96112179hg19UCSC Ensembl
Innerchr3:97561554..97594869hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3833316
hg1933316
hg1833316
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893750
Supporting Variants
Samples
Known GenesMIR8060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780331
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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