A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556034



Internal ID18410424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11928745..11934994hg38UCSC Ensembl
Outerchr19:11928186..11935685hg38UCSC Ensembl
Innerchr19:12039560..12045809hg19UCSC Ensembl
Outerchr19:12039001..12046500hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754781
Samples
Known GenesZNF700
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556034
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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