A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021029



Internal ID22082660
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156615
Supporting Variants
Samples
Known GenesLCE3D, LCE3E
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021029
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer