A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544941



Internal ID18746017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:75389585..75395925hg38UCSC Ensembl
Outerchr9:75389085..75397084hg38UCSC Ensembl
Innerchr9:78004501..78010841hg19UCSC Ensembl
Outerchr9:78004001..78012000hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743688
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544941
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer