A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780576



Internal ID19177647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166576511..166641371hg38UCSC Ensembl
Innerchr1:166545748..166610608hg19UCSC Ensembl
Innerchr1:164812372..164877232hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3864861
hg1964861
hg1864861
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890737
Supporting Variants
Samples
Known GenesFMO9P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780576
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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