A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778467



Internal ID18833947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4034049..4094550hg38UCSC Ensembl
Innerchr3:4075733..4136234hg19UCSC Ensembl
Innerchr3:4050733..4111234hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3860502
hg1960502
hg1860502
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893636
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778467
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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