A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556698



Internal ID18757774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58455273..58469487hg38UCSC Ensembl
Outerchr19:58454784..58470569hg38UCSC Ensembl
Innerchr19:58966640..58980854hg19UCSC Ensembl
Outerchr19:58966151..58981936hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3815786
hg1915786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755445
Samples
Known GenesZNF324, ZNF324B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556698
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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