A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790795



Internal ID19169220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196841868..196927958hg38UCSC Ensembl
Innerchr1:196810998..196897088hg19UCSC Ensembl
Innerchr1:195077621..195163711hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3886091
hg1986091
hg1886091
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890993
Supporting Variants
Samples
Known GenesCFHR4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790795
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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