A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952080



Internal ID16954267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89982593..90047992hg38UCSC Ensembl
Outerchr16:90049001..90114400hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3865400
hg1965400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000199
SamplesBILGI_BIOE
Known GenesAFG3L1P, C16orf3, DBNDD1, GAS8, URAHP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952080
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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