A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998702



Internal ID16944968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:15559192..15579191hg38UCSC Ensembl
Outerchr8:15416701..15436700hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3820000
hg1920000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951108
Supporting Variants
SamplesBILGI_BIOE
Known GenesTUSC3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998702
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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