A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562718



Internal ID18763794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150160298..150160587hg38UCSC Ensembl
Outerchr3:150160241..150160645hg38UCSC Ensembl
Innerchr3:149878085..149878374hg19UCSC Ensembl
Outerchr3:149878028..149878432hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761465
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562718
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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