A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893328



Internal ID19184148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26145712..26320138hg38UCSC Ensembl
Outerchr20:26029592..26320138hg38UCSC Ensembl
Innerchr20:26126348..26300774hg19UCSC Ensembl
Outerchr20:26010228..26300774hg19UCSC Ensembl
Innerchr20:26074348..26248774hg18UCSC Ensembl
Outerchr20:25958228..26248774hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38290547
hg19290547
hg18290547
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791304, essv25791862, essv25792881
Samples
Known GenesFAM182A, LOC284801, MIR663A, NCOR1P1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893328
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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