A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893164



Internal ID19183984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12075946..12113357hg38UCSC Ensembl
Outerchr19:12075946..12113357hg38UCSC Ensembl
Innerchr19:12186761..12224172hg19UCSC Ensembl
Outerchr19:12186761..12224172hg19UCSC Ensembl
Innerchr19:12047761..12085172hg18UCSC Ensembl
Outerchr19:12047761..12085172hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3837412
hg1937412
hg1837412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783604, essv25798719, essv25781465
Samples
Known GenesZNF788, ZNF844
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893164
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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