A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556035



Internal ID18410425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11931676..11932386hg38UCSC Ensembl
Outerchr19:11931557..11932427hg38UCSC Ensembl
Innerchr19:12042491..12043201hg19UCSC Ensembl
Outerchr19:12042372..12043242hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754782
Samples
Known GenesZNF700
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556035
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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