A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156615



Internal ID22087016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152554167..152583051hg38UCSC Ensembl
Outerchr1:152546733..152583230hg38UCSC Ensembl
Innerchr1:152526643..152555527hg19UCSC Ensembl
Outerchr1:152519209..152555706hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3836498
hg1936498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021029
Samples
Known GenesLCE3D, LCE3E
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156615
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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