A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562334



Internal ID18763410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106038548..106038669hg38UCSC Ensembl
Outerchr3:106038544..106038672hg38UCSC Ensembl
Innerchr3:105757395..105757516hg19UCSC Ensembl
Outerchr3:105757391..105757519hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761081
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562334
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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