A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9759147



Internal ID18733393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156220621..156220810hg38UCSC Ensembl
Outerchr2:156220580..156220861hg38UCSC Ensembl
Innerchr2:157077133..157077322hg19UCSC Ensembl
Outerchr2:157077092..157077373hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3560400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9759147
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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