A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9743929



Internal ID18718175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98266473..98266797hg38UCSC Ensembl
Outerchr9:98266425..98266847hg38UCSC Ensembl
Innerchr9:101028755..101029079hg19UCSC Ensembl
Outerchr9:101028707..101029129hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9743929
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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