A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006660



Internal ID22068291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72892228..72965839hg38UCSC Ensembl
Outerchr9:72889101..72976317hg38UCSC Ensembl
Innerchr9:75507144..75580755hg19UCSC Ensembl
Outerchr9:75504017..75591233hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3887217
hg1987217
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154512
Supporting Variants
Samples
Known GenesALDH1A1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006660
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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