A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007860



Internal ID22069491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:200994038..201011943hg38UCSC Ensembl
Outerchr1:200991758..201014120hg38UCSC Ensembl
Innerchr1:200963166..200981071hg19UCSC Ensembl
Outerchr1:200960886..200983248hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3822363
hg1922363
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154560
Supporting Variants
Samples
Known GenesKIF21B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007860
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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