A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3562794



Internal ID18417184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159711212..159711393hg38UCSC Ensembl
Outerchr3:159711174..159711446hg38UCSC Ensembl
Innerchr3:159429001..159429182hg19UCSC Ensembl
Outerchr3:159428963..159429235hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9761541
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3562794
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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