A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006659



Internal ID22068290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72811005..72850359hg38UCSC Ensembl
Outerchr9:72805473..72853515hg38UCSC Ensembl
Innerchr9:75425921..75465275hg19UCSC Ensembl
Outerchr9:75420389..75468431hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3848043
hg1948043
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154511
Supporting Variants
Samples
Known GenesTMC1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006659
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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