A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007758



Internal ID22069389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113122418..113142540hg38UCSC Ensembl
Outerchr9:113121473..113143557hg38UCSC Ensembl
Innerchr9:115884698..115904820hg19UCSC Ensembl
Outerchr9:115883753..115905837hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3822085
hg1922085
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154534
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007758
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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