A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562777



Internal ID18763853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158399136..158399448hg38UCSC Ensembl
Outerchr3:158399082..158399494hg38UCSC Ensembl
Innerchr3:158116925..158117237hg19UCSC Ensembl
Outerchr3:158116871..158117283hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761524
Samples
Known GenesRSRC1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562777
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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