A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544901



Internal ID18745977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71654479..71654746hg38UCSC Ensembl
Outerchr9:71654443..71654802hg38UCSC Ensembl
Innerchr9:74269395..74269662hg19UCSC Ensembl
Outerchr9:74269359..74269718hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743648
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544901
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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