A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154517



Internal ID22085022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:82761656..82769329hg38UCSC Ensembl
Outerchr9:82749856..82776771hg38UCSC Ensembl
Innerchr9:85376571..85384244hg19UCSC Ensembl
Outerchr9:85364771..85391686hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3826916
hg1926916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006668
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154517
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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