A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743688



Internal ID18717934
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 StatusS
Merged Variantsesv3544941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743688
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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