A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155381



Internal ID22085886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16329903..16390256hg38UCSC Ensembl
Outerchr17:16325984..16391221hg38UCSC Ensembl
Innerchr17:16233217..16293570hg19UCSC Ensembl
Outerchr17:16229298..16294535hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3865238
hg1965238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4010111
Samples
Known GenesCENPV, PIGL, UBB
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155381
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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