A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010111



Internal ID22071742
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155381
Supporting Variants
Samples
Known GenesCENPV, PIGL, UBB
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010111
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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