A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955409



Internal ID17304282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:39291892..39292494hg38UCSC Ensembl
Outerchr17:37448145..37448747hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001524
SamplesBILGI_BIOE
Known GenesFBXL20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955409
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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