A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562958



Internal ID18764034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177663713..177667641hg38UCSC Ensembl
Outerchr3:177663367..177667800hg38UCSC Ensembl
Innerchr3:177381501..177385429hg19UCSC Ensembl
Outerchr3:177381155..177385588hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384434
hg194434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761705
Samples
Known GenesLINC00578
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562958
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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