A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3556338



Internal ID18410728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36350191..36355947hg38UCSC Ensembl
Outerchr19:36349099..36356444hg38UCSC Ensembl
Innerchr19:36841093..36846849hg19UCSC Ensembl
Outerchr19:36840001..36847346hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg387346
hg197346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755085
Samples
Known GenesZFP14
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3556338
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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