A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154446



Internal ID22084951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:186251537..186278792hg38UCSC Ensembl
Outerchr1:186247620..186286162hg38UCSC Ensembl
Innerchr1:186220669..186247924hg19UCSC Ensembl
Outerchr1:186216752..186255294hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3838543
hg1938543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005222
Samples
Known GenesMIR548F1, RNU6-72P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154446
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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