A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007756



Internal ID22069387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113092071..113122780hg38UCSC Ensembl
Outerchr9:113058286..113125832hg38UCSC Ensembl
Innerchr9:115854351..115885060hg19UCSC Ensembl
Outerchr9:115820566..115888112hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3867547
hg1967547
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154533
Supporting Variants
Samples
Known GenesFAM225A, FAM225B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007756
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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