A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893155



Internal ID18837289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:725939..797079hg38UCSC Ensembl
Outerchr19:725939..804013hg38UCSC Ensembl
Innerchr19:725939..797079hg19UCSC Ensembl
Outerchr19:725939..804013hg19UCSC Ensembl
Innerchr19:676939..748079hg18UCSC Ensembl
Outerchr19:676939..755013hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3878075
hg1978075
hg1878075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789025, essv25789356
Samples
Known GenesMISP, PALM, PTBP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893155
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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