A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006656



Internal ID22068287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482739..69503518hg38UCSC Ensembl
Outerchr9:69476351..69505204hg38UCSC Ensembl
Innerchr9:72097655..72118434hg19UCSC Ensembl
Outerchr9:72091267..72120120hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3828854
hg1928854
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154508
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006656
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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