A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005289



Internal ID22066920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30620842..30702069hg38UCSC Ensembl
Outerchr9:30620331..30708218hg38UCSC Ensembl
Innerchr9:30620840..30702067hg19UCSC Ensembl
Outerchr9:30620329..30708216hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3887888
hg1987888
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154477
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005289
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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