A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789356



Internal ID18822801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:725939..797079hg38UCSC Ensembl
Innerchr19:725939..797079hg19UCSC Ensembl
Innerchr19:676939..748079hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3871141
hg1971141
hg1871141
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893155
Supporting Variants
Samples
Known GenesMISP, PALM
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789356
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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