A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022975



Internal ID22084606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162342537..162386350hg38UCSC Ensembl
Outerchr1:162342037..162386602hg38UCSC Ensembl
Innerchr1:162312327..162356140hg19UCSC Ensembl
Outerchr1:162311827..162356392hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3844566
hg1944566
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156839
Supporting Variants
Samples
Known GenesC1orf111, C1orf226, MIR556, NOS1AP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022975
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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