A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893177



Internal ID18837311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20605819..20831597hg38UCSC Ensembl
Outerchr19:20605819..20831597hg38UCSC Ensembl
Innerchr19:20788625..21014403hg19UCSC Ensembl
Outerchr19:20788625..21014403hg19UCSC Ensembl
Innerchr19:20580465..20806243hg18UCSC Ensembl
Outerchr19:20580465..20806243hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38225779
hg19225779
hg18225779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792453
Samples
Known GenesZNF626
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893177
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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