A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154495



Internal ID22085000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41533431..41623340hg38UCSC Ensembl
Outerchr9:41480799..41639957hg38UCSC Ensembl
Innerchr9:45616520..45706444hg19UCSC Ensembl
Outerchr9:45556556..45723034hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38159159
hg19166479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005451
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154495
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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