A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893163



Internal ID18837297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11017920..11063949hg38UCSC Ensembl
Outerchr19:11017920..11063949hg38UCSC Ensembl
Innerchr19:11128596..11174625hg19UCSC Ensembl
Outerchr19:11128596..11174625hg19UCSC Ensembl
Innerchr19:10989596..11035625hg18UCSC Ensembl
Outerchr19:10989596..11035625hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3846030
hg1946030
hg1846030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788487
Samples
Known GenesSMARCA4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893163
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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