A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156341



Internal ID22084817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108966266..109196558hg38UCSC Ensembl
Outerchr1:108962290..109197926hg38UCSC Ensembl
Innerchr1:109508888..109739180hg19UCSC Ensembl
Outerchr1:109504912..109740548hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38235637
hg19235637
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021415
Samples
Known GenesC1orf194, CLCC1, KIAA1324, SCARNA2, TAF13, TMEM167B, WDR47
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156341
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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