A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785694



Internal ID18814087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143674158..144572337hg38UCSC Ensembl
Innerchr1:149168798..149512609hg19UCSC Ensembl
Innerchr1:147435422..147779233hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38898180
hg19343812
hg18343812
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894156
Supporting Variants
Samples
Known GenesFCGR1C, LOC388692
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785694
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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