A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022973



Internal ID22084604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162116588..162223948hg38UCSC Ensembl
Outerchr1:162112032..162224708hg38UCSC Ensembl
Innerchr1:162086378..162193738hg19UCSC Ensembl
Outerchr1:162081822..162194498hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38112677
hg19112677
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156831
Supporting Variants
Samples
Known GenesMIR4654, NOS1AP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022973
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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