A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788698



Internal ID18831849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:251309..275462hg38UCSC Ensembl
Innerchr3:292992..317145hg19UCSC Ensembl
Innerchr3:267992..292145hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3824154
hg1924154
hg1824154
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893589
Supporting Variants
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788698
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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