A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016337



Internal ID22077968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31814142..32274915hg38UCSC Ensembl
Outerchr3:31813264..32278021hg38UCSC Ensembl
Innerchr3:31855634..32316407hg19UCSC Ensembl
Outerchr3:31854756..32319513hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38464758
hg19464758
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155957
Supporting Variants
Samples
Known GenesCMTM8, GPD1L, OSBPL10, ZNF860
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016337
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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